2-171247983-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171247983
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171247983
    reference: chr 2
allele count: 1
allele frequency: 1.696928559307653e-5
allele num: 58930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-47A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-47A>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16830
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5940
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

2-171247994-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171247994
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171247994
    reference: chr 2
allele count: 2
allele frequency: 3.288824574097218e-5
allele num: 60812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-36A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-36A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22350
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6852
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5635
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

2-171248008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248008
    reference: chr 2
allele count: 1
allele frequency: 1.525041176111755e-5
allele num: 65572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-22C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-22C>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3804
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

2-171248010-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248010
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248010
    reference: chr 2
allele count: 1
allele frequency: 1.487519709636153e-5
allele num: 67226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-20A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-20A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4512
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23156
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

2-171248010-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248010
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248010
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 67226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-20A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-20A>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22555
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-171248015-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248015
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248015
    reference: chr 2
allele count: 1
allele frequency: 1.39388363859385e-5
allele num: 71742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-15C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-15C>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

2-171248017-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248017
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248018
    reference: chr 2
allele count: 451
allele frequency: 7.993902655180971e-3
allele num: 56418
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-4dupT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-4dupT
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 2.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 14437
  bin: 2.25e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 14538
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8869
  bin: 1.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 1.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 4.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 5.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 7.5e0
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 4.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 3.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 6.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 1.25e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 14746
  bin: 2.25e1
  variant carriers: 68
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-171248017-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248017
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248016
    reference: chr 2
allele count: 51
allele frequency: 9.039668191002871e-4
allele num: 56418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-4delT
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-4delT
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 8869
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 14437
  bin: 2.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2188
  bin: 1.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 10718
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 1.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 3.75e1
  variant carriers: 10
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: CT
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-171248019-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248019
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248019
    reference: chr 2
allele count: 34
allele frequency: 4.176493710691824e-4
allele num: 81408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-11T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-11T>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16182
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7650
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6666
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2669
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 9.75e1
  variant carriers: 34
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

2-171248019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248019
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248019
    reference: chr 2
allele count: 1
allele frequency: 1.228380503144654e-5
allele num: 81408
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-11T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-11T>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7650
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3433
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2669
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-171248022-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248022
    reference: chr 2
allele count: 5
allele frequency: 5.544835540177878e-5
allele num: 90174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1605-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1578-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1721-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1721-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1446-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1578-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1605-8T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1578-8T>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18671
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1578-8T>C
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-171248034-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248034
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248034
    reference: chr 2
allele count: 1
allele frequency: 1.006684384311831e-5
allele num: 99336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1725G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1609G>C
  hgvsp: ENSP00000335100.6:p.Glu537Gln
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1609G>C
  hgvsp: ENSP00000446237.1:p.Glu537Gln
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1450G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1725G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1582G>C
  hgvsp: ENSP00000386497.3:p.Glu528Gln
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1582G>C
  hgvsp: ENSP00000314650.6:p.Glu528Gln
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1582G>C
  hgvsp: ENSP00000386213.4:p.Glu528Gln
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu528Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/2-171248041-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248041
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248041
    reference: chr 2
allele count: 1
allele frequency: 9.678855572117152e-6
allele num: 103318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1589A>C
  hgvsp: ENSP00000314650.6:p.Asn530Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1732A>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1457A>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1589A>C
  hgvsp: ENSP00000386497.3:p.Asn530Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1589A>C
  hgvsp: ENSP00000386213.4:p.Asn530Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1616A>C
  hgvsp: ENSP00000446237.1:p.Asn539Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1732A>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1616A>C
  hgvsp: ENSP00000335100.6:p.Asn539Thr
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3787
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn530Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

2-171248049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248049
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248049
    reference: chr 2
allele count: 1
allele frequency: 9.278847938239988e-6
allele num: 107772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1465A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1740A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1624A>G
  hgvsp: ENSP00000446237.1:p.Ile542Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1597A>G
  hgvsp: ENSP00000386213.4:p.Ile533Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1740A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1597A>G
  hgvsp: ENSP00000314650.6:p.Ile533Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1597A>G
  hgvsp: ENSP00000386497.3:p.Ile533Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1624A>G
  hgvsp: ENSP00000335100.6:p.Ile542Val
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile533Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-171248052-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248052
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248052
    reference: chr 2
allele count: 1
allele frequency: 9.102494083378845e-6
allele num: 109860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1627T>A
  hgvsp: ENSP00000446237.1:p.Phe543Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1600T>A
  hgvsp: ENSP00000386213.4:p.Phe534Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1468T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1743T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1627T>A
  hgvsp: ENSP00000335100.6:p.Phe543Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1743T>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1600T>A
  hgvsp: ENSP00000314650.6:p.Phe534Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1600T>A
  hgvsp: ENSP00000386497.3:p.Phe534Ile
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe534Ile
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

2-171248055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248055
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248055
    reference: chr 2
allele count: 4
allele frequency: 3.561253561253561e-5
allele num: 112320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1603T>C
  hgvsp: ENSP00000314650.6:p.Tyr535His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1746T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1746T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1603T>C
  hgvsp: ENSP00000386497.3:p.Tyr535His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1471T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1630T>C
  hgvsp: ENSP00000446237.1:p.Tyr544His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1603T>C
  hgvsp: ENSP00000386213.4:p.Tyr535His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1630T>C
  hgvsp: ENSP00000335100.6:p.Tyr544His
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44202
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr535His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

2-171248058-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248058
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248058
    reference: chr 2
allele count: 1
allele frequency: 8.755647392568207e-6
allele num: 114212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1749T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1474T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1633T>C
  hgvsp: ENSP00000335100.6:p.Tyr545His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1606T>C
  hgvsp: ENSP00000386213.4:p.Tyr536His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1749T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1606T>C
  hgvsp: ENSP00000386497.3:p.Tyr536His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1606T>C
  hgvsp: ENSP00000314650.6:p.Tyr536His
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1633T>C
  hgvsp: ENSP00000446237.1:p.Tyr545His
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr536His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-171248059-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248059
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248059
    reference: chr 2
allele count: 2
allele frequency: 1.742980147456121e-5
allele num: 114746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1634A>G
  hgvsp: ENSP00000446237.1:p.Tyr545Cys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1607A>G
  hgvsp: ENSP00000386497.3:p.Tyr536Cys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1750A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1634A>G
  hgvsp: ENSP00000335100.6:p.Tyr545Cys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1607A>G
  hgvsp: ENSP00000314650.6:p.Tyr536Cys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1750A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1607A>G
  hgvsp: ENSP00000386213.4:p.Tyr536Cys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1475A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr536Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-171248061-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248061
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248061
    reference: chr 2
allele count: 1
allele frequency: 8.639607416239006e-6
allele num: 115746
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1609A>G
  hgvsp: ENSP00000386213.4:p.Ile537Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1477A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1752A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1609A>G
  hgvsp: ENSP00000386497.3:p.Ile537Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1609A>G
  hgvsp: ENSP00000314650.6:p.Ile537Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1752A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1636A>G
  hgvsp: ENSP00000446237.1:p.Ile546Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1636A>G
  hgvsp: ENSP00000335100.6:p.Ile546Val
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46663
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile537Val
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-171248062-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248062
    reference: chr 2
allele count: 2
allele frequency: 1.722237531000276e-5
allele num: 116128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1478T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1753T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1610T>C
  hgvsp: ENSP00000314650.6:p.Ile537Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1610T>C
  hgvsp: ENSP00000386497.3:p.Ile537Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1637T>C
  hgvsp: ENSP00000335100.6:p.Ile546Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1753T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1610T>C
  hgvsp: ENSP00000386213.4:p.Ile537Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1637T>C
  hgvsp: ENSP00000446237.1:p.Ile546Thr
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46870
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile537Thr
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-171248071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248071
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248071
    reference: chr 2
allele count: 5
allele frequency: 4.217060540121114e-5
allele num: 118566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1646G>A
  hgvsp: ENSP00000335100.6:p.Gly549Asp
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1619G>A
  hgvsp: ENSP00000386213.4:p.Gly540Asp
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1619G>A
  hgvsp: ENSP00000314650.6:p.Gly540Asp
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1619G>A
  hgvsp: ENSP00000386497.3:p.Gly540Asp
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1646G>A
  hgvsp: ENSP00000446237.1:p.Gly549Asp
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1762G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1487G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1762G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly540Asp
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-171248076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248076
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248076
    reference: chr 2
allele count: 1
allele frequency: 8.405197774303629e-6
allele num: 118974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1651C>T
  hgvsp: ENSP00000446237.1:p.His551Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1624C>T
  hgvsp: ENSP00000314650.6:p.His542Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1624C>T
  hgvsp: ENSP00000386497.3:p.His542Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1767C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1624C>T
  hgvsp: ENSP00000386213.4:p.His542Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1767C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1651C>T
  hgvsp: ENSP00000335100.6:p.His551Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1492C>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His542Tyr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-171248106-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248106
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248106
    reference: chr 2
allele count: 1
allele frequency: 8.379560575843403e-6
allele num: 119338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1522C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1681C>A
  hgvsp: ENSP00000335100.6:p.Leu561Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1654C>A
  hgvsp: ENSP00000386497.3:p.Leu552Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1681C>A
  hgvsp: ENSP00000446237.1:p.Leu561Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1654C>A
  hgvsp: ENSP00000314650.6:p.Leu552Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1654C>A
  hgvsp: ENSP00000386213.4:p.Leu552Ile
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1797C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1797C>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu552Ile
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-171248108-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248108
    reference: chr 2
allele count: 1
allele frequency: 8.381246123673667e-6
allele num: 119314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1683T>G
  hgvsp: ENST00000334231.6:c.1683T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1656T>G
  hgvsp: ENST00000409044.3:c.1656T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1656T>G
  hgvsp: ENST00000317935.6:c.1656T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1683T>G
  hgvsp: ENST00000484338.2:c.1683T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1799T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1656T>G
  hgvsp: ENST00000408978.4:c.1656T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1799T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1524T>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu552Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-171248108-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248107
    reference: chr 2
allele count: 2
allele frequency: 1.676249224734733e-5
allele num: 119314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1658delC
  hgvsp: ENSP00000314650.6:p.Pro553LeufsTer9
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1801delC
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1658delC
  hgvsp: ENSP00000386213.4:p.Pro553LeufsTer9
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1685delC
  hgvsp: ENSP00000446237.1:p.Pro562LeufsTer9
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1685delC
  hgvsp: ENSP00000335100.6:p.Pro562LeufsTer9
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1658delC
  hgvsp: ENSP00000386497.3:p.Pro553LeufsTer9
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1801delC
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1526delC
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro553LeufsTer9
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: TC
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

2-171248112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248112
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248112
    reference: chr 2
allele count: 17
allele frequency: 1.426174496644295e-4
allele num: 119200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1660G>A
  hgvsp: ENSP00000386497.3:p.Glu554Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1687G>A
  hgvsp: ENSP00000446237.1:p.Glu563Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1803G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1803G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1528G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1660G>A
  hgvsp: ENSP00000386213.4:p.Glu554Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1660G>A
  hgvsp: ENSP00000314650.6:p.Glu554Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1687G>A
  hgvsp: ENSP00000335100.6:p.Glu563Lys
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39233
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu554Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

2-171248115-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248115
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248114
    reference: chr 2
allele count: 2
allele frequency: 1.680700515975058e-5
allele num: 118998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1695delA
  hgvsp: ENSP00000335100.6:p.Lys565AsnfsTer6
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1695delA
  hgvsp: ENSP00000446237.1:p.Lys565AsnfsTer6
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1811delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1668delA
  hgvsp: ENSP00000386497.3:p.Lys556AsnfsTer6
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1668delA
  hgvsp: ENSP00000386213.4:p.Lys556AsnfsTer6
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1668delA
  hgvsp: ENSP00000314650.6:p.Lys556AsnfsTer6
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1536delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1811delA
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys556AsnfsTer6
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: GA
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-171248124-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248124
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248124
    reference: chr 2
allele count: 2
allele frequency: 1.689988508078145e-5
allele num: 118344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1699C>G
  hgvsp: ENSP00000335100.6:p.Pro567Ala
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1540C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1672C>G
  hgvsp: ENSP00000386497.3:p.Pro558Ala
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1699C>G
  hgvsp: ENSP00000446237.1:p.Pro567Ala
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1815C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1672C>G
  hgvsp: ENSP00000314650.6:p.Pro558Ala
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1672C>G
  hgvsp: ENSP00000386213.4:p.Pro558Ala
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1815C>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro558Ala
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-171248128-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248128
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248128
    reference: chr 2
allele count: 1
allele frequency: 8.485218748939348e-6
allele num: 117852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676G>C
  hgvsp: ENSP00000386213.4:p.Arg559Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703G>C
  hgvsp: ENSP00000335100.6:p.Arg568Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676G>C
  hgvsp: ENSP00000314650.6:p.Arg559Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676G>C
  hgvsp: ENSP00000386497.3:p.Arg559Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703G>C
  hgvsp: ENSP00000446237.1:p.Arg568Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819G>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg559Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-171248137-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248137
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248135
    reference: chr 2
allele count: 1
allele frequency: 8.605703860518751e-6
allele num: 116202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+10_1819+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+10_1819+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+10_1703+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+10_1703+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+10_1676+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+10_1676+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+10_1676+11delAG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+10_1544+11delAG
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CAG
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-171248138-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248138
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248139
    reference: chr 2
allele count: 1
allele frequency: 8.621878879845495e-6
allele num: 115984
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+16dupG
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+16dupG
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32291
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4758
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40278
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

2-171248139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248139
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248139
    reference: chr 2
allele count: 2
allele frequency: 1.726728023069086e-5
allele num: 115826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+11G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+11G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-171248147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248147
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248147
    reference: chr 2
allele count: 1
allele frequency: 8.713382012094175e-6
allele num: 114766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+19G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+19G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

2-171248148-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248148
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248148
    reference: chr 2
allele count: 3
allele frequency: 2.615518744551003e-5
allele num: 114700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+20G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+20G>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

2-171248152-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248152
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248152
    reference: chr 2
allele count: 2
allele frequency: 1.749566982171912e-5
allele num: 114314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+24T>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+24T>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4165
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-171248161-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248161
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248161
    reference: chr 2
allele count: 5
allele frequency: 4.414309425433485e-5
allele num: 113268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+33G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+33G>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19439
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4756
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-171248166-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248166
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248166
    reference: chr 2
allele count: 1
allele frequency: 8.897747090436701e-6
allele num: 112388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+38A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+38A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16019
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7034
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8183
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-171248167-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248167
    reference: chr 2
allele count: 8
allele frequency: 7.121492664862555e-5
allele num: 112336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+39T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+39T>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14230
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7023
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

2-171248168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248168
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248168
    reference: chr 2
allele count: 11
allele frequency: 9.827570803180559e-5
allele num: 111930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+40G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13424
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14845
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15618
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

2-171248171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248171
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248171
    reference: chr 2
allele count: 1
allele frequency: 9.02380479705463e-6
allele num: 110818
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+43C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+43C>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15580
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7805
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3097
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

2-171248172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248172
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248172
    reference: chr 2
allele count: 4
allele frequency: 3.61755236407047e-5
allele num: 110572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1676+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1703+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1703+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1676+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1544+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1676+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1819+44G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1819+44G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13222
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7728
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-171248842-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248842
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248842
    reference: chr 2
allele count: 1
allele frequency: 8.834546611067921e-6
allele num: 113192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-49C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-49C>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13189
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4608
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

2-171248849-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248849
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248849
    reference: chr 2
allele count: 1
allele frequency: 8.80266192496611e-6
allele num: 113602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-42A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-42A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-171248851-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248851
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248851
    reference: chr 2
allele count: 1
allele frequency: 8.800647727672756e-6
allele num: 113628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-40T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-40T>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16933
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2492
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5831
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

2-171248865-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248865
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248865
    reference: chr 2
allele count: 29
allele frequency: 2.532264543057229e-4
allele num: 114522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-26G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-26G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21027
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17994
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

2-171248869-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248869
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248869
    reference: chr 2
allele count: 1
allele frequency: 8.712015611931977e-6
allele num: 114784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-22G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-22G>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-171248874-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248874
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248874
    reference: chr 2
allele count: 2
allele frequency: 1.734454947532738e-5
allele num: 115310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-17T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-17T>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37365
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-171248878-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248878
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248878
    reference: chr 2
allele count: 7
allele frequency: 6.043235030043511e-5
allele num: 115832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1545-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1704-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1677-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1677-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1820-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1704-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1677-13C>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1820-13C>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18809
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22730
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

2-171248894-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248894
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248894
    reference: chr 2
allele count: 1
allele frequency: 8.497476249553883e-6
allele num: 117682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1680C>G
  hgvsp: ENSP00000386497.3:p.Tyr560Ter
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1707C>G
  hgvsp: ENSP00000446237.1:p.Tyr569Ter
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1823C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1548C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1707C>G
  hgvsp: ENSP00000335100.6:p.Tyr569Ter
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1823C>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1680C>G
  hgvsp: ENSP00000314650.6:p.Tyr560Ter
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1680C>G
  hgvsp: ENSP00000386213.4:p.Tyr560Ter
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr560Ter
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-171248895-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248895
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248895
    reference: chr 2
allele count: 1
allele frequency: 8.48824378236143e-6
allele num: 117810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1681A>G
  hgvsp: ENSP00000314650.6:p.Ile561Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1708A>G
  hgvsp: ENSP00000446237.1:p.Ile570Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1824A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1824A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1681A>G
  hgvsp: ENSP00000386497.3:p.Ile561Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1549A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1708A>G
  hgvsp: ENSP00000335100.6:p.Ile570Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1681A>G
  hgvsp: ENSP00000386213.4:p.Ile561Val
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24615
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile561Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

2-171248896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248896
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248896
    reference: chr 2
allele count: 1
allele frequency: 8.482051978014521e-6
allele num: 117896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1682T>C
  hgvsp: ENSP00000386497.3:p.Ile561Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1709T>C
  hgvsp: ENSP00000446237.1:p.Ile570Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1550T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1682T>C
  hgvsp: ENSP00000314650.6:p.Ile561Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1825T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1825T>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1682T>C
  hgvsp: ENSP00000386213.4:p.Ile561Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1709T>C
  hgvsp: ENSP00000335100.6:p.Ile570Thr
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile561Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

2-171248924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248924
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248924
    reference: chr 2
allele count: 4
allele frequency: 3.349354411937099e-5
allele num: 119426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1737C>T
  hgvsp: ENST00000334231.6:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1578C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1853C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1737C>T
  hgvsp: ENST00000484338.2:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1710C>T
  hgvsp: ENST00000409044.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1710C>T
  hgvsp: ENST00000408978.4:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1853C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1710C>T
  hgvsp: ENST00000317935.6:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4594
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His570His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

2-171248925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248925
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248925
    reference: chr 2
allele count: 2
allele frequency: 1.674312694638851e-5
allele num: 119452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1738G>A
  hgvsp: ENSP00000335100.6:p.Asp580Asn
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1579G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1854G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1738G>A
  hgvsp: ENSP00000446237.1:p.Asp580Asn
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1711G>A
  hgvsp: ENSP00000386213.4:p.Asp571Asn
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1711G>A
  hgvsp: ENSP00000314650.6:p.Asp571Asn
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1711G>A
  hgvsp: ENSP00000386497.3:p.Asp571Asn
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1854G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp571Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-171248925-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248925
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248925
    reference: chr 2
allele count: 8
allele frequency: 6.697250778555402e-5
allele num: 119452
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1711G>T
  hgvsp: ENSP00000386213.4:p.Asp571Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1854G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1579G>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1738G>T
  hgvsp: ENSP00000335100.6:p.Asp580Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1711G>T
  hgvsp: ENSP00000314650.6:p.Asp571Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1711G>T
  hgvsp: ENSP00000386497.3:p.Asp571Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1738G>T
  hgvsp: ENSP00000446237.1:p.Asp580Tyr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1854G>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25490
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20415
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp571Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

2-171248928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248928
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248928
    reference: chr 2
allele count: 3
allele frequency: 2.510334209161046e-5
allele num: 119506
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1582A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1857A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1741A>G
  hgvsp: ENSP00000446237.1:p.Ile581Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1714A>G
  hgvsp: ENSP00000386497.3:p.Ile572Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1714A>G
  hgvsp: ENSP00000386213.4:p.Ile572Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1714A>G
  hgvsp: ENSP00000314650.6:p.Ile572Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1741A>G
  hgvsp: ENSP00000335100.6:p.Ile581Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1857A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6407
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile572Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-171248928-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248928
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248928
    reference: chr 2
allele count: 24
allele frequency: 2.008267367328837e-4
allele num: 119506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1857A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1857A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1714A>T
  hgvsp: ENSP00000314650.6:p.Ile572Leu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1714A>T
  hgvsp: ENSP00000386213.4:p.Ile572Leu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1714A>T
  hgvsp: ENSP00000386497.3:p.Ile572Leu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1582A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1741A>T
  hgvsp: ENSP00000446237.1:p.Ile581Leu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1741A>T
  hgvsp: ENSP00000335100.6:p.Ile581Leu
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25493
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20459
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4614
  bin: 9.75e1
  variant carriers: 24
hgvs: p.Ile572Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-171248952-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248952
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248952
    reference: chr 2
allele count: 1
allele frequency: 8.377173876620983e-6
allele num: 119372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1765A>G
  hgvsp: ENSP00000335100.6:p.Arg589Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1881A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1881A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1765A>G
  hgvsp: ENSP00000446237.1:p.Arg589Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1606A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1738A>G
  hgvsp: ENSP00000386213.4:p.Arg580Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1738A>G
  hgvsp: ENSP00000386497.3:p.Arg580Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1738A>G
  hgvsp: ENSP00000314650.6:p.Arg580Gly
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4590
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg580Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

2-171248957-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248957
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248957
    reference: chr 2
allele count: 1
allele frequency: 8.391092016715055e-6
allele num: 119174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1886A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1743A>G
  hgvsp: ENST00000317935.6:c.1743A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1743A>G
  hgvsp: ENST00000409044.3:c.1743A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1770A>G
  hgvsp: ENST00000484338.2:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1886A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1770A>G
  hgvsp: ENST00000334231.6:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1611A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1743A>G
  hgvsp: ENST00000408978.4:c.1743A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6306
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln581Gln
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-171248960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248960
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248960
    reference: chr 2
allele count: 22
allele frequency: 1.846195159611963e-4
allele num: 119164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1614C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1773C>T
  hgvsp: ENST00000484338.2:c.1773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1746C>T
  hgvsp: ENST00000317935.6:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1889C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1773C>T
  hgvsp: ENST00000334231.6:c.1773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1746C>T
  hgvsp: ENST00000409044.3:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1889C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1746C>T
  hgvsp: ENST00000408978.4:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20649
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24857
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe582Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-171248961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248961
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248961
    reference: chr 2
allele count: 232
allele frequency: 1.946668009196328e-3
allele num: 119178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1774G>A
  hgvsp: ENSP00000446237.1:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1747G>A
  hgvsp: ENSP00000314650.6:p.Glu583Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1774G>A
  hgvsp: ENSP00000335100.6:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1747G>A
  hgvsp: ENSP00000386497.3:p.Glu583Lys
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1615G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1890G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1890G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1747G>A
  hgvsp: ENSP00000386213.4:p.Glu583Lys
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 20641
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 24792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 4729
  bin: 9.75e1
  variant carriers: 231
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42297
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu583Lys
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

2-171248964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248964
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248964
    reference: chr 2
allele count: 1
allele frequency: 8.408307407718826e-6
allele num: 118930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1893G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1893G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1750G>A
  hgvsp: ENSP00000314650.6:p.Ala584Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1777G>A
  hgvsp: ENSP00000446237.1:p.Ala593Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1750G>A
  hgvsp: ENSP00000386497.3:p.Ala584Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1777G>A
  hgvsp: ENSP00000335100.6:p.Ala593Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1750G>A
  hgvsp: ENSP00000386213.4:p.Ala584Thr
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1618G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6280
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala584Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-171248974-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248974
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248974
    reference: chr 2
allele count: 1
allele frequency: 8.461525443807009e-6
allele num: 118182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1760A>G
  hgvsp: ENSP00000386497.3:p.His587Arg
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1787A>G
  hgvsp: ENSP00000446237.1:p.His596Arg
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1903A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1760A>G
  hgvsp: ENSP00000314650.6:p.His587Arg
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1760A>G
  hgvsp: ENSP00000386213.4:p.His587Arg
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1628A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1787A>G
  hgvsp: ENSP00000335100.6:p.His596Arg
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1903A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20516
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His587Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

2-171248992-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248992
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248992
    reference: chr 2
allele count: 2
allele frequency: 1.726817475392851e-5
allele num: 115820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1778G>A
  hgvsp: ENSP00000386497.3:p.Gly593Glu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1646G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1805G>A
  hgvsp: ENSP00000446237.1:p.Gly602Glu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1805G>A
  hgvsp: ENSP00000335100.6:p.Gly602Glu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1778G>A
  hgvsp: ENSP00000314650.6:p.Gly593Glu
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1921G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1921G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1778G>A
  hgvsp: ENSP00000386213.4:p.Gly593Glu
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3975
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly593Glu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-171248993-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248993
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248993
    reference: chr 2
allele count: 1
allele frequency: 8.64707815229234e-6
allele num: 115646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1922G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1779G>C
  hgvsp: ENST00000317935.6:c.1779G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1779G>C
  hgvsp: ENST00000408978.4:c.1779G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1779G>C
  hgvsp: ENST00000409044.3:c.1779G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1806G>C
  hgvsp: ENST00000484338.2:c.1806G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1647G>C
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1806G>C
  hgvsp: ENST00000334231.6:c.1806G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1922G>C
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4535
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6068
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly593Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

2-171248996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248996
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248996
    reference: chr 2
allele count: 4
allele frequency: 3.474031613687685e-5
allele num: 115140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1925C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1782C>T
  hgvsp: ENST00000408978.4:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1809C>T
  hgvsp: ENST00000484338.2:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1782C>T
  hgvsp: ENST00000409044.3:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1809C>T
  hgvsp: ENST00000334231.6:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1925C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1782C>T
  hgvsp: ENST00000317935.6:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1650C>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19759
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe594Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

2-171248998-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248998
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248998
    reference: chr 2
allele count: 1
allele frequency: 8.710042679209128e-6
allele num: 114810
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1784C>T
  hgvsp: ENSP00000386213.4:p.Thr595Met
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1784C>T
  hgvsp: ENSP00000386497.3:p.Thr595Met
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1784C>T
  hgvsp: ENSP00000314650.6:p.Thr595Met
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1811C>T
  hgvsp: ENSP00000446237.1:p.Thr604Met
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1652C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1927C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1927C>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1811C>T
  hgvsp: ENSP00000335100.6:p.Thr604Met
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6015
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr595Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-171248999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171248999
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171248999
    reference: chr 2
allele count: 5
allele frequency: 4.360718646432932e-5
allele num: 114660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1785G>A
  hgvsp: ENST00000317935.6:c.1785G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1785G>A
  hgvsp: ENST00000409044.3:c.1785G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1812G>A
  hgvsp: ENST00000484338.2:c.1812G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1785G>A
  hgvsp: ENST00000408978.4:c.1785G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1812G>A
  hgvsp: ENST00000334231.6:c.1812G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1928G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1928G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1653G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4910
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37325
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr595Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

2-171249001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171249001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171249001
    reference: chr 2
allele count: 1
allele frequency: 8.736065974770241e-6
allele num: 114468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1814A>G
  hgvsp: ENSP00000335100.6:p.Asp605Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1930A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1814A>G
  hgvsp: ENSP00000446237.1:p.Asp605Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1930A>G
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1787A>G
  hgvsp: ENSP00000314650.6:p.Asp596Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1787A>G
  hgvsp: ENSP00000386497.3:p.Asp596Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1787A>G
  hgvsp: ENSP00000386213.4:p.Asp596Gly
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1655A>G
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp596Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

2-171249001-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171249001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171249001
    reference: chr 2
allele count: 3
allele frequency: 2.620819792431072e-5
allele num: 114468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1814A>T
  hgvsp: ENSP00000335100.6:p.Asp605Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1787A>T
  hgvsp: ENSP00000314650.6:p.Asp596Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1787A>T
  hgvsp: ENSP00000386213.4:p.Asp596Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1930A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1814A>T
  hgvsp: ENSP00000446237.1:p.Asp605Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1655A>T
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1787A>T
  hgvsp: ENSP00000386497.3:p.Asp596Val
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1930A>T
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19590
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp596Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-171249010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171249010
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171249010
    reference: chr 2
allele count: 1
allele frequency: 8.847521809141259e-6
allele num: 113026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1934+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1818+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1791+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1791+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1818+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1934+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1791+5G>A
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1659+5G>A
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1791+5G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

2-171249023-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 171249023
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 171249022
    reference: chr 2
allele count: 11
allele frequency: 9.970631956781843e-5
allele num: 110324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386497
  ensembl transcript: ENST00000409044
  gene symbol: MYO3B
  hgvsc: ENST00000409044.3:c.1791+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000386213
  ensembl transcript: ENST00000408978
  gene symbol: MYO3B
  hgvsc: ENST00000408978.4:c.1791+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000602629
  gene symbol: MYO3B
  hgvsc: ENST00000602629.1:n.1659+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000438642
  gene symbol: MYO3B
  hgvsc: ENST00000438642.2:n.1934+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl transcript: ENST00000409940
  gene symbol: MYO3B
  hgvsc: ENST00000409940.2:n.1934+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000446237
  ensembl transcript: ENST00000484338
  gene symbol: MYO3B
  hgvsc: ENST00000484338.2:c.1818+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000314650
  ensembl transcript: ENST00000317935
  gene symbol: MYO3B
  hgvsc: ENST00000317935.6:c.1791+19delA
  variant of: http://identifiers.org/hgnc/15576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071909
  ensembl protein: ENSP00000335100
  ensembl transcript: ENST00000334231
  gene symbol: MYO3B
  hgvsc: ENST00000334231.6:c.1818+19delA
  variant of: http://identifiers.org/hgnc/15576
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18114
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 1
num of homozygotes: 0
reference allele: GA

GenotypeQuality
all individuals: 5185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7064
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4764
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15648
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.2e-5
allele num: 31250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.002e0

DP
type: SiteQuality
SIO_000300: 7.6309e5

QD
type: SiteQuality
SIO_000300: 1.054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

GenotypeQuality
all individuals: 379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4343
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.200012400024801e-5
allele num: 32258
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.534e0

DP
type: SiteQuality
SIO_000300: 8.0221e5

GenotypeQuality
all individuals: 4463
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23096
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5020
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.880682145532062e-5
allele num: 34714
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

DP
type: SiteQuality
SIO_000300: 9.08042e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.477e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

GenotypeQuality
all individuals: 248
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6112
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.325581395348837e-4
allele num: 4300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.586e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

DP
type: SiteQuality
SIO_000300: 9.34867e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeQuality
all individuals: 650
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4512
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4300
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.586e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 9.34867e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

GenotypeQuality
all individuals: 381
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 400
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38032
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.151012891344383e-4
allele num: 8688
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.97677e5

QD
type: SiteQuality
SIO_000300: 6.74e0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.517e-1

GenotypeQuality
all individuals: 10718
bin: 2.5e0
variant carriers: 56

GenotypeQuality
all individuals: 2188
bin: 1.75e1
variant carriers: 99

GenotypeQuality
all individuals: 988
bin: 5.25e1
variant carriers: 24

GenotypeQuality
all individuals: 9593
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 3262
bin: 3.25e1
variant carriers: 82

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3325
bin: 2.75e1
variant carriers: 92

GenotypeQuality
all individuals: 406
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 363
bin: 7.25e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 195
allele frequency: 6.453961739590918e-3
allele num: 30214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 3.785830178474851e-3
allele num: 3698
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 6.838608831574834e-3
allele num: 5118
num of homozygotes: 0

Latino
type: Population
allele count: 39
allele frequency: 5.624459186616672e-3
allele num: 6934
num of homozygotes: 0

South Asian
type: Population
allele count: 129
allele frequency: 2.027664256523106e-2
allele num: 6362
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 1.004016064257028e-2
allele num: 498
num of homozygotes: 0

East Asian
type: Population
allele count: 34
allele frequency: 9.460211463550361e-3
allele num: 3594
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.157084e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 1.432e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

QD
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeQuality
all individuals: 9593
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1026
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1287
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1631
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3262
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 14746
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 905
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 2.75e1
variant carriers: 6

African
type: Population
allele count: 5
allele frequency: 9.769441187964048e-4
allele num: 5118
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 8.347245409015025e-4
allele num: 3594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 1.026014430396505e-3
allele num: 30214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3698
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 1.100282929896259e-3
allele num: 6362
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.326507066628209e-4
allele num: 6934
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 4.016064257028112e-3
allele num: 498
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.157084e6

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 1.432e0

QD
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
all individuals: 3433
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15118
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2024
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 927
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16445
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 24
allele frequency: 2.524721228697665e-3
allele num: 9506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 2.083622725378525e-4
allele num: 43194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.483679525222552e-3
allele num: 674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

DP
type: SiteQuality
SIO_000300: 1.142409e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

GenotypeQuality
all individuals: 1947
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2479
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.315136361531694e-5
allele num: 43194
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.142409e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

QD
type: SiteQuality
SIO_000300: 1.254e1

GenotypeQuality
all individuals: 1714
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1023
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.338329764453962e-4
allele num: 7472
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5254
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.63907556138338e-4
allele num: 12202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.080386119663809e-5
allele num: 48068
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

DP
type: SiteQuality
SIO_000300: 1.159485e6

FS
type: SiteQuality
SIO_000300: 5.436e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

QD
type: SiteQuality
SIO_000300: 1.463e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
all individuals: 9993
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.26427429899753e-5
allele num: 13766
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.280757e6

QD
type: SiteQuality
SIO_000300: 6.8e0

VQSLOD
type: SiteQuality
SIO_000300: -6.964e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8195
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.385041551246538e-4
allele num: 7220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

FS
type: SiteQuality
SIO_000300: 6.608e0

MQRankSum
type: SiteQuality
SIO_000300: -1.674e0

QD
type: SiteQuality
SIO_000300: 2.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.323e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.331153e6

GenotypeQuality
all individuals: 659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 820
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.012256669069935e-5
allele num: 11096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15116
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.932e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

QD
type: SiteQuality
SIO_000300: 1.401e1

DP
type: SiteQuality
SIO_000300: 1.388586e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5399
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 504
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42100
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.13869278068777e-4
allele num: 8782
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.589e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.067e-1

FS
type: SiteQuality
SIO_000300: 1.996e0

DP
type: SiteQuality
SIO_000300: 1.411625e6

GenotypeQuality
all individuals: 1191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.552435868033942e-5
allele num: 61046
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.435735e6

FS
type: SiteQuality
SIO_000300: 3.007e0

QD
type: SiteQuality
SIO_000300: 1.68e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.838607035531201e-5
allele num: 11314
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62272
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

FS
type: SiteQuality
SIO_000300: 4.237e0

DP
type: SiteQuality
SIO_000300: 1.45493e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
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SIO_000300: 1.258e1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

VQSLOD
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SIO_000300: 1.02e0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.193255843658194e-5
allele num: 62632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

FS
type: SiteQuality
SIO_000300: 5.329e0

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

DP
type: SiteQuality
SIO_000300: 1.461036e6

QD
type: SiteQuality
SIO_000300: 1.875e1

VQSLOD
type: SiteQuality
SIO_000300: -5.999999999999999e-4

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-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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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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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.071581654522075e-4
allele num: 9332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63314
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16108
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.814e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.322e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.057e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

DP
type: SiteQuality
SIO_000300: 1.471148e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.146831141040972e-5
allele num: 63556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 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: 6482
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

FS
type: SiteQuality
SIO_000300: 5.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

QD
type: SiteQuality
SIO_000300: 1.345e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

DP
type: SiteQuality
SIO_000300: 1.474849e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.364525139664804e-4
allele num: 11456
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65278
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.500236e6

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

GenotypeQuality
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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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bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65584
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.139e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 1.504351e6

BaseQRankSum
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SIO_000300: -1.732e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65846
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.50808e6

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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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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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519387383007172e-5
allele num: 65816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038774766014343e-5
allele num: 65816
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.507067e6

MQRankSum
type: SiteQuality
SIO_000300: -1.039e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

QD
type: SiteQuality
SIO_000300: 1.405e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65742
num of homozygotes: 0

African
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allele count: 12
allele frequency: 1.250260470931444e-3
allele num: 9598
num of homozygotes: 0

Latino
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allele count: 5
allele frequency: 4.35691878703381e-4
allele num: 11476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.072e0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.505786e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-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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variant carriers: 0

African
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allele count: 2
allele frequency: 2.088991017338625e-4
allele num: 9574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65622
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 3.341e0

DP
type: SiteQuality
SIO_000300: 1.502834e6

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

QD
type: SiteQuality
SIO_000300: 2.088e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

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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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.224889759921607e-4
allele num: 16328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65176
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.38e0

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.490468e6

QD
type: SiteQuality
SIO_000300: 1.175e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-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
all individuals: 295
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64844
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.138735420503377e-5
allele num: 16290
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.479055e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

FS
type: SiteQuality
SIO_000300: 1.313e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.44e-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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bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.197318007662835e-4
allele num: 8352
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63700
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.635e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.197e0

QD
type: SiteQuality
SIO_000300: 1.662e1

MQ
type: SiteQuality
SIO_000300: 5.996e1

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 1.273e0

DP
type: SiteQuality
SIO_000300: 1.431571e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573762236001385e-5
allele num: 63542
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.23e0

MQRankSum
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 1.42605e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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Latino
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allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.152187618207036e-5
allele num: 63448
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
SIO_000300: 4.453e0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.594082764777147e-5
allele num: 62732
num of homozygotes: 0

South Asian
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Other
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East Asian
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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BaseQRankSum
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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: 3

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.646086533787069e-4
allele num: 8228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

FS
type: SiteQuality
SIO_000300: 2.025e0

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.439e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 1.360614e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

GenotypeQuality
all individuals: 680
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 5.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.203690651630679e-5
allele num: 62428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.556e1

DP
type: SiteQuality
SIO_000300: 1.332405e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1967
bin: 9.75e1
variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.81257930034439e-4
allele num: 11034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.860661049902787e-5
allele num: 61720
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.673e0

QD
type: SiteQuality
SIO_000300: 1.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

DP
type: SiteQuality
SIO_000300: 1.268136e6

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
all individuals: 2864
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61064
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.30119722747322e-5
allele num: 15870
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.228589e6

VQSLOD
type: SiteQuality
SIO_000300: -1.784e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

QD
type: SiteQuality
SIO_000300: 1.598e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeQuality
all individuals: 3910
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8219
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variant carriers: 0

GenotypeQuality
all individuals: 679
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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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: 1008
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variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.310615989515072e-4
allele num: 61040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.139e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

FS
type: SiteQuality
SIO_000300: 2.859e0

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.928e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.228324e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
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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: 1972
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variant carriers: 11

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9146
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.262785705265816e-4
allele num: 15838
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.121914734480179e-3
allele num: 8022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10970
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.265e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.313e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 2.453e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.223234e6

GenotypeQuality
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bin: 2.5e0
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
all individuals: 672
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GenotypeQuality
all individuals: 1962
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.214891264283081e-5
allele num: 10852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60052
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.211e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 1963
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variant carriers: 3

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 6951
bin: 3.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14472
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.339009649737888e-5
allele num: 59898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.589825119236884e-4
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.36213258684311e-5
allele num: 15718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.208144e6

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 9.606e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

VQSLOD
type: SiteQuality
SIO_000300: -1.671e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
SIO_000300: 4.71e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566465114821893e-5
allele num: 63838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

QD
type: SiteQuality
SIO_000300: 3.166e1

MQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.478e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.557785e6

VQSLOD
type: SiteQuality
SIO_000300: -3.718e0

GenotypeQuality
all individuals: 330
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variant carriers: 0

GenotypeQuality
all individuals: 2582
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variant carriers: 0

GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 1075
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GenotypeQuality
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GenotypeQuality
all individuals: 5839
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30010
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GenotypeQuality
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GenotypeQuality
all individuals: 1717
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GenotypeQuality
all individuals: 4601
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variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9546
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64002
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.474e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.885e1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.835e-1

DP
type: SiteQuality
SIO_000300: 1.579428e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.226e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30516
bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562207086171343e-5
allele num: 64012
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.584946e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ReadPosRankSum
type: SiteQuality
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QD
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.99e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.794944256389553e-4
allele num: 64402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

Latino
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allele count: 9
allele frequency: 7.867132867132868e-4
allele num: 11440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.380952380952381e-3
allele num: 840
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13334
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.299e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.631149e6

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.114e0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

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

South Asian
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allele count: 1
allele frequency: 7.447125409591897e-5
allele num: 13428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

DP
type: SiteQuality
SIO_000300: 1.639789e6

QD
type: SiteQuality
SIO_000300: 1.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -3.265e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.588e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.469507714915503e-4
allele num: 13610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.48e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.651949e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-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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variant carriers: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.076658053402239e-4
allele num: 65016
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.48e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.334e0

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.119e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519202722411279e-5
allele num: 65824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.022e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

FS
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
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num of homozygotes: 0

African
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 65852
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South Asian
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East Asian
type: Population
allele count: 0
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.043318348998774e-4
allele num: 9788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.725115e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

FS
type: SiteQuality
SIO_000300: 8.92e-1

QD
type: SiteQuality
SIO_000300: 1.169e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6392
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
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: 15790
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.125e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

DP
type: SiteQuality
SIO_000300: 1.725696e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

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

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.514526710402999e-4
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.333122229259025e-5
allele num: 15790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.031363088057901e-5
allele num: 66320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

FS
type: SiteQuality
SIO_000300: 1.125e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

QD
type: SiteQuality
SIO_000300: 1.411e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

DP
type: SiteQuality
SIO_000300: 1.725696e6

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

GenotypeQuality
all individuals: 42603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4614
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 3
allele frequency: 2.604166666666667e-4
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.726597e6

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

FS
type: SiteQuality
SIO_000300: 1.112e0

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

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

GenotypeQuality
all individuals: 42603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 24
allele frequency: 1.515917129863567e-3
allele num: 15832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

FS
type: SiteQuality
SIO_000300: 1.112e0

QD
type: SiteQuality
SIO_000300: 1.389e1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.726597e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

DP
type: SiteQuality
SIO_000300: 1.72522e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 6.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

FS
type: SiteQuality
SIO_000300: 1.415e0

QD
type: SiteQuality
SIO_000300: 1.062e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 1043
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41986
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.39467962655071e-5
allele num: 15638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.722944e6

MQRankSum
type: SiteQuality
SIO_000300: -1.127e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.462e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

QD
type: SiteQuality
SIO_000300: 7.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66216
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
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: 9786
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.27942681678608e-3
allele num: 15632
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.253e1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 1.723896e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510026576467746e-5
allele num: 66224
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.81657113079729e-4
allele num: 11514
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

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

African
type: Population
allele count: 221
allele frequency: 2.258789860997547e-2
allele num: 9784
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 1.734125e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4535
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511395925276585e-5
allele num: 66164
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15468
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

FS
type: SiteQuality
SIO_000300: 1.086e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.521e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

BaseQRankSum
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SIO_000300: -1.083e0

DP
type: SiteQuality
SIO_000300: 1.718167e6

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.664001066240171e-5
allele num: 15006
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: 0
allele frequency: 0.0e0
allele num: 65918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.757e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.70597e6

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 5.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.022e-1

BaseQRankSum
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SIO_000300: 3.25e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.745810055865922e-4
allele num: 11456
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65034
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9708
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.669766e6

FS
type: SiteQuality
SIO_000300: 9.815e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

VQSLOD
type: SiteQuality
SIO_000300: -2.025e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.106e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-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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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64966
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.031353135313531e-4
allele num: 9696
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.0456e1

VQSLOD
type: SiteQuality
SIO_000300: -6.272e-1

DP
type: SiteQuality
SIO_000300: 1.667329e6

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.61e-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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variant carriers: 0

South Asian
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allele count: 4
allele frequency: 2.992667963489451e-4
allele num: 13366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64760
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0402e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.279e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.65e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.669e0

DP
type: SiteQuality
SIO_000300: 1.661697e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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: 9664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547700117625209e-5
allele num: 64612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.929e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

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

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.492e0

DP
type: SiteQuality
SIO_000300: 1.657052e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.744316194473592e-5
allele num: 11436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.106876553438277e-4
allele num: 9656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549810923067386e-5
allele num: 64524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7126e1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.18595825426945e-4
allele num: 8432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64452
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
type: SiteQuality
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FS
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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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: 3
allele frequency: 4.654626698938745e-5
allele num: 64452
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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BaseQRankSum
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QD
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FS
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
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VQSLOD
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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
all individuals: 5874
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567348985925206e-5
allele num: 63802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.929e0

FS
type: SiteQuality
SIO_000300: 1.1512e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.728e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 1.625248e6

QD
type: SiteQuality
SIO_000300: 5.94e0