X-31462758-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462758
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462758
    reference: chr 0
allele count: 3
allele frequency: 3.448791198684861e-5
allele num: 86987
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-14A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-14A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15802
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

X-31462759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462759
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462759
    reference: chr 0
allele count: 3
allele frequency: 3.449584325088827e-5
allele num: 86967
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-15G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-15G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
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genotype depth: GenotypeDepth
  all individuals: 2276
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2706
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

X-31462762-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462762
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462762
    reference: chr 0
allele count: 1
allele frequency: 1.150867178418939e-5
allele num: 86891
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-18T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-18T>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1281
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-31462768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462768
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462768
    reference: chr 0
allele count: 1
allele frequency: 1.152511899685364e-5
allele num: 86767
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-24T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-31462769-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462769
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462769
    reference: chr 0
allele count: 2
allele frequency: 2.305980560583874e-5
allele num: 86731
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-25A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-25A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2890
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
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genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23932
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 3549
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-31462774-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462774
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462774
    reference: chr 0
allele count: 1
allele frequency: 1.154641079820338e-5
allele num: 86607
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-30T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-30T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1928
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
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genotype depth: GenotypeDepth
  all individuals: 4134
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1967
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genotype quality: GenotypeQuality
  all individuals: 2159
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genotype quality: GenotypeQuality
  all individuals: 290
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

X-31462788-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031462788
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031462788
    reference: chr 0
allele count: 1
allele frequency: 1.163792100179224e-5
allele num: 85926
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8938-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2026-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1558-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1558-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8926-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1558-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1558-44T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1558-44T>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

X-31496180-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496180
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496180
    reference: chr 0
allele count: 3
allele frequency: 4.358627903935841e-5
allele num: 68829
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+43A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2865
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 9411
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genotype depth: GenotypeDepth
  all individuals: 349
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genotype depth: GenotypeDepth
  all individuals: 36
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genotype depth: GenotypeDepth
  all individuals: 545
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8473
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

X-31496187-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496187
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496187
    reference: chr 0
allele count: 1
allele frequency: 1.446842988598877e-5
allele num: 69116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+36A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+36A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 249
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 545
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 81
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genotype depth: GenotypeDepth
  all individuals: 177
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1161
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

X-31496195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496195
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496195
    reference: chr 0
allele count: 2
allele frequency: 2.869852202611566e-5
allele num: 69690
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+28C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+28C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14749
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
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genotype depth: GenotypeDepth
  all individuals: 545
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 81
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genotype depth: GenotypeDepth
  all individuals: 110
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
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genotype quality: GenotypeQuality
  all individuals: 3706
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 837
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genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

X-31496196-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496196
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496197
    reference: chr 0
allele count: 1
allele frequency: 1.434144102799449e-5
allele num: 69728
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+26dupG
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+26dupG
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
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genotype quality: GenotypeQuality
  all individuals: 704
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 15133
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

X-31496213-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496213
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496213
    reference: chr 0
allele count: 1
allele frequency: 1.396726074082351e-5
allele num: 71596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+10A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+10A>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-31496213-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496213
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496213
    reference: chr 0
allele count: 1
allele frequency: 1.396726074082351e-5
allele num: 71596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+10A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+10A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 406
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 521
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genotype quality: GenotypeQuality
  all individuals: 76
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-31496217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496217
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496217
    reference: chr 0
allele count: 1
allele frequency: 1.389178301034938e-5
allele num: 71985
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+6G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+6G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19568
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 56
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
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genotype quality: GenotypeQuality
  all individuals: 1388
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
hgvs: c.8937+6G>A
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

X-31496218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496218
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496218
    reference: chr 0
allele count: 1
allele frequency: 1.386039807063259e-5
allele num: 72148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1557+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1557+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1557+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2025+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8937+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1557+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8925+5C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1557+5C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19546
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3606
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
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genotype depth: GenotypeDepth
  all individuals: 110
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 520
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
hgvs: c.8937+5C>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

X-31496229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496229
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496229
    reference: chr 0
allele count: 1
allele frequency: 1.362564892152989e-5
allele num: 73391
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2019A>G
  hgvsp: ENST00000358062.2:c.2019A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8919A>G
  hgvsp: ENST00000378677.2:c.8919A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1551A>G
  hgvsp: ENST00000343523.2:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1551A>G
  hgvsp: ENST00000541735.1:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1551A>G
  hgvsp: ENST00000474231.1:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8931A>G
  hgvsp: ENST00000357033.4:c.8931A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1551A>G
  hgvsp: ENST00000378707.3:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1551A>G
  hgvsp: ENST00000359836.1:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4790
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys2977Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

X-31496234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496234
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496234
    reference: chr 0
allele count: 2
allele frequency: 2.710761724044456e-5
allele num: 73780
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8926G>A
  hgvsp: ENSP00000354923.3:p.Glu2976Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1546G>A
  hgvsp: ENSP00000340057.2:p.Glu516Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1546G>A
  hgvsp: ENSP00000417123.1:p.Glu516Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1546G>A
  hgvsp: ENSP00000367979.3:p.Glu516Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2014G>A
  hgvsp: ENSP00000350765.2:p.Glu672Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8914G>A
  hgvsp: ENSP00000367948.2:p.Glu2972Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1546G>A
  hgvsp: ENSP00000444119.1:p.Glu516Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1546G>A
  hgvsp: ENSP00000352894.1:p.Glu516Lys
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19997
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20017
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu2976Lys
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: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff

X-31496235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496235
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496235
    reference: chr 0
allele count: 4
allele frequency: 5.404382954576162e-5
allele num: 74014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1545C>T
  hgvsp: ENST00000541735.1:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1545C>T
  hgvsp: ENST00000343523.2:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8913C>T
  hgvsp: ENST00000378677.2:c.8913C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2013C>T
  hgvsp: ENST00000358062.2:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1545C>T
  hgvsp: ENST00000378707.3:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8925C>T
  hgvsp: ENST00000357033.4:c.8925C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1545C>T
  hgvsp: ENST00000359836.1:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1545C>T
  hgvsp: ENST00000474231.1:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20096
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu2975Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

X-31496235-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496235
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496235
    reference: chr 0
allele count: 1
allele frequency: 1.35109573864404e-5
allele num: 74014
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8925C>G
  hgvsp: ENST00000357033.4:c.8925C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8913C>G
  hgvsp: ENST00000378677.2:c.8913C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1545C>G
  hgvsp: ENST00000343523.2:c.1545C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1545C>G
  hgvsp: ENST00000378707.3:c.1545C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1545C>G
  hgvsp: ENST00000474231.1:c.1545C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1545C>G
  hgvsp: ENST00000541735.1:c.1545C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2013C>G
  hgvsp: ENST00000358062.2:c.2013C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1545C>G
  hgvsp: ENST00000359836.1:c.1545C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4022
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu2975Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

X-31496247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496247
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496247
    reference: chr 0
allele count: 1
allele frequency: 1.332817977048874e-5
allele num: 75029
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8901C>T
  hgvsp: ENST00000378677.2:c.8901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.2001C>T
  hgvsp: ENST00000358062.2:c.2001C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1533C>T
  hgvsp: ENST00000378707.3:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1533C>T
  hgvsp: ENST00000343523.2:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1533C>T
  hgvsp: ENST00000474231.1:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1533C>T
  hgvsp: ENST00000359836.1:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1533C>T
  hgvsp: ENST00000541735.1:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8913C>T
  hgvsp: ENST00000357033.4:c.8913C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu2971Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

X-31496252-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496252
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496252
    reference: chr 0
allele count: 1
allele frequency: 1.326435866825839e-5
allele num: 75390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1996T>C
  hgvsp: ENSP00000350765.2:p.Ser666Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8908T>C
  hgvsp: ENSP00000354923.3:p.Ser2970Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1528T>C
  hgvsp: ENSP00000352894.1:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1528T>C
  hgvsp: ENSP00000367979.3:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1528T>C
  hgvsp: ENSP00000340057.2:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1528T>C
  hgvsp: ENSP00000444119.1:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8896T>C
  hgvsp: ENSP00000367948.2:p.Ser2966Pro
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1528T>C
  hgvsp: ENSP00000417123.1:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser2970Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-31496257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496257
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496257
    reference: chr 0
allele count: 2
allele frequency: 2.641903227084792e-5
allele num: 75703
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8903T>C
  hgvsp: ENSP00000354923.3:p.Ile2968Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1523T>C
  hgvsp: ENSP00000352894.1:p.Ile508Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8891T>C
  hgvsp: ENSP00000367948.2:p.Ile2964Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1523T>C
  hgvsp: ENSP00000444119.1:p.Ile508Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1523T>C
  hgvsp: ENSP00000367979.3:p.Ile508Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1991T>C
  hgvsp: ENSP00000350765.2:p.Ile664Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1523T>C
  hgvsp: ENSP00000417123.1:p.Ile508Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1523T>C
  hgvsp: ENSP00000340057.2:p.Ile508Thr
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile2968Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

X-31496265-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496265
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496265
    reference: chr 0
allele count: 1
allele frequency: 1.313766964015923e-5
allele num: 76117
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1515T>A
  hgvsp: ENSP00000352894.1:p.Asp505Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1515T>A
  hgvsp: ENSP00000417123.1:p.Asp505Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1515T>A
  hgvsp: ENSP00000340057.2:p.Asp505Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8895T>A
  hgvsp: ENSP00000354923.3:p.Asp2965Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1515T>A
  hgvsp: ENSP00000367979.3:p.Asp505Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1515T>A
  hgvsp: ENSP00000444119.1:p.Asp505Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1983T>A
  hgvsp: ENSP00000350765.2:p.Asp661Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8883T>A
  hgvsp: ENSP00000367948.2:p.Asp2961Glu
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp2965Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-31496267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496267
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496267
    reference: chr 0
allele count: 3
allele frequency: 3.943891569274455e-5
allele num: 76067
alternate allele: T
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8893G>A
  hgvsp: ENSP00000354923.3:p.Asp2965Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8881G>A
  hgvsp: ENSP00000367948.2:p.Asp2961Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1513G>A
  hgvsp: ENSP00000340057.2:p.Asp505Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1513G>A
  hgvsp: ENSP00000444119.1:p.Asp505Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1513G>A
  hgvsp: ENSP00000417123.1:p.Asp505Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1981G>A
  hgvsp: ENSP00000350765.2:p.Asp661Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1513G>A
  hgvsp: ENSP00000352894.1:p.Asp505Asn
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1513G>A
  hgvsp: ENSP00000367979.3:p.Asp505Asn
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 9.25e1
  variant carriers: 1
hgvs: p.Asp2965Asn
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS

X-31496273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496273
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496273
    reference: chr 0
allele count: 1
allele frequency: 1.3042060645582e-5
allele num: 76675
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1507G>A
  hgvsp: ENSP00000417123.1:p.Val503Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1507G>A
  hgvsp: ENSP00000340057.2:p.Val503Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1975G>A
  hgvsp: ENSP00000350765.2:p.Val659Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1507G>A
  hgvsp: ENSP00000444119.1:p.Val503Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1507G>A
  hgvsp: ENSP00000367979.3:p.Val503Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8875G>A
  hgvsp: ENSP00000367948.2:p.Val2959Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8887G>A
  hgvsp: ENSP00000354923.3:p.Val2963Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1507G>A
  hgvsp: ENSP00000352894.1:p.Val503Met
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4822
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2932
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3302
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val2963Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-31496274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496274
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496274
    reference: chr 0
allele count: 2
allele frequency: 2.604132758688038e-5
allele num: 76801
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8886C>T
  hgvsp: ENST00000357033.4:c.8886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1506C>T
  hgvsp: ENST00000541735.1:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1506C>T
  hgvsp: ENST00000378707.3:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1974C>T
  hgvsp: ENST00000358062.2:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8874C>T
  hgvsp: ENST00000378677.2:c.8874C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1506C>T
  hgvsp: ENST00000343523.2:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1506C>T
  hgvsp: ENST00000474231.1:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1506C>T
  hgvsp: ENST00000359836.1:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2201
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro2962Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

X-31496275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496275
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496275
    reference: chr 0
allele count: 6
allele frequency: 7.787757644982089e-5
allele num: 77044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1505C>T
  hgvsp: ENSP00000352894.1:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1505C>T
  hgvsp: ENSP00000444119.1:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1505C>T
  hgvsp: ENSP00000340057.2:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8873C>T
  hgvsp: ENSP00000367948.2:p.Pro2958Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1505C>T
  hgvsp: ENSP00000417123.1:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1973C>T
  hgvsp: ENSP00000350765.2:p.Pro658Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8885C>T
  hgvsp: ENSP00000354923.3:p.Pro2962Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1505C>T
  hgvsp: ENSP00000367979.3:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18592
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro2962Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

X-31496299-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496299
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496299
    reference: chr 0
allele count: 1
allele frequency: 1.2567076772272e-5
allele num: 79573
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8861A>T
  hgvsp: ENSP00000354923.3:p.Glu2954Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8849A>T
  hgvsp: ENSP00000367948.2:p.Glu2950Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1949A>T
  hgvsp: ENSP00000350765.2:p.Glu650Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1481A>T
  hgvsp: ENSP00000352894.1:p.Glu494Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1481A>T
  hgvsp: ENSP00000340057.2:p.Glu494Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1481A>T
  hgvsp: ENSP00000367979.3:p.Glu494Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1481A>T
  hgvsp: ENSP00000444119.1:p.Glu494Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1481A>T
  hgvsp: ENSP00000417123.1:p.Glu494Val
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21229
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu2954Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-31496302-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496302
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496302
    reference: chr 0
allele count: 1
allele frequency: 1.254295963675589e-5
allele num: 79726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1478C>A
  hgvsp: ENSP00000352894.1:p.Ala493Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1478C>A
  hgvsp: ENSP00000340057.2:p.Ala493Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8858C>A
  hgvsp: ENSP00000354923.3:p.Ala2953Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8846C>A
  hgvsp: ENSP00000367948.2:p.Ala2949Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1946C>A
  hgvsp: ENSP00000350765.2:p.Ala649Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1478C>A
  hgvsp: ENSP00000444119.1:p.Ala493Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1478C>A
  hgvsp: ENSP00000417123.1:p.Ala493Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1478C>A
  hgvsp: ENSP00000367979.3:p.Ala493Asp
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala2953Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

X-31496304-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496304
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496304
    reference: chr 0
allele count: 3
allele frequency: 3.750140630273635e-5
allele num: 79997
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1476A>G
  hgvsp: ENST00000359836.1:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8844A>G
  hgvsp: ENST00000378677.2:c.8844A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1476A>G
  hgvsp: ENST00000343523.2:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8856A>G
  hgvsp: ENST00000357033.4:c.8856A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1476A>G
  hgvsp: ENST00000474231.1:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1476A>G
  hgvsp: ENST00000378707.3:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1476A>G
  hgvsp: ENST00000541735.1:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1944A>G
  hgvsp: ENST00000358062.2:c.1944A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4863
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 21423
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln2952Gln
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

X-31496304-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496304
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496304
    reference: chr 0
allele count: 1
allele frequency: 1.250046876757878e-5
allele num: 79997
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1476A>C
  hgvsp: ENSP00000444119.1:p.Gln492His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1476A>C
  hgvsp: ENSP00000367979.3:p.Gln492His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1476A>C
  hgvsp: ENSP00000340057.2:p.Gln492His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8856A>C
  hgvsp: ENSP00000354923.3:p.Gln2952His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1476A>C
  hgvsp: ENSP00000352894.1:p.Gln492His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1476A>C
  hgvsp: ENSP00000417123.1:p.Gln492His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1944A>C
  hgvsp: ENSP00000350765.2:p.Gln648His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8844A>C
  hgvsp: ENSP00000367948.2:p.Gln2948His
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4863
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln2952His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

X-31496308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496308
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496308
    reference: chr 0
allele count: 8
allele frequency: 9.961399576640517e-5
allele num: 80310
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1472G>A
  hgvsp: ENSP00000417123.1:p.Arg491His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1472G>A
  hgvsp: ENSP00000444119.1:p.Arg491His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1472G>A
  hgvsp: ENSP00000352894.1:p.Arg491His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1472G>A
  hgvsp: ENSP00000340057.2:p.Arg491His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1472G>A
  hgvsp: ENSP00000367979.3:p.Arg491His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1940G>A
  hgvsp: ENSP00000350765.2:p.Arg647His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8852G>A
  hgvsp: ENSP00000354923.3:p.Arg2951His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8840G>A
  hgvsp: ENSP00000367948.2:p.Arg2947His
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg2951His
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS

X-31496309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496309
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496309
    reference: chr 0
allele count: 3
allele frequency: 3.726476616359232e-5
allele num: 80505
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1939C>T
  hgvsp: ENSP00000350765.2:p.Arg647Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1471C>T
  hgvsp: ENSP00000367979.3:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1471C>T
  hgvsp: ENSP00000444119.1:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8851C>T
  hgvsp: ENSP00000354923.3:p.Arg2951Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1471C>T
  hgvsp: ENSP00000340057.2:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8839C>T
  hgvsp: ENSP00000367948.2:p.Arg2947Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1471C>T
  hgvsp: ENSP00000417123.1:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1471C>T
  hgvsp: ENSP00000352894.1:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg2951Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

X-31496313-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496313
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496313
    reference: chr 0
allele count: 1
allele frequency: 1.233197681588359e-5
allele num: 81090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1467G>A
  hgvsp: ENST00000343523.2:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1467G>A
  hgvsp: ENST00000541735.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8835G>A
  hgvsp: ENST00000378677.2:c.8835G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1467G>A
  hgvsp: ENST00000474231.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1935G>A
  hgvsp: ENST00000358062.2:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8847G>A
  hgvsp: ENST00000357033.4:c.8847G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1467G>A
  hgvsp: ENST00000378707.3:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1467G>A
  hgvsp: ENST00000359836.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys2949Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-31496324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496324
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496324
    reference: chr 0
allele count: 1
allele frequency: 1.214181641573579e-5
allele num: 82360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1456C>T
  hgvsp: ENST00000378707.3:c.1456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1456C>T
  hgvsp: ENST00000474231.1:c.1456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1456C>T
  hgvsp: ENST00000359836.1:c.1456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1456C>T
  hgvsp: ENST00000541735.1:c.1456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1456C>T
  hgvsp: ENST00000343523.2:c.1456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1924C>T
  hgvsp: ENST00000358062.2:c.1924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8836C>T
  hgvsp: ENST00000357033.4:c.8836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8824C>T
  hgvsp: ENST00000378677.2:c.8824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25062
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu2946Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

X-31496329-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496329
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496329
    reference: chr 0
allele count: 1
allele frequency: 1.204253423090355e-5
allele num: 83039
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1451A>G
  hgvsp: ENSP00000417123.1:p.Asp484Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1451A>G
  hgvsp: ENSP00000352894.1:p.Asp484Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8831A>G
  hgvsp: ENSP00000354923.3:p.Asp2944Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1451A>G
  hgvsp: ENSP00000444119.1:p.Asp484Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8819A>G
  hgvsp: ENSP00000367948.2:p.Asp2940Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1919A>G
  hgvsp: ENSP00000350765.2:p.Asp640Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1451A>G
  hgvsp: ENSP00000340057.2:p.Asp484Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1451A>G
  hgvsp: ENSP00000367979.3:p.Asp484Gly
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4945
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp2944Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

X-31496331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496331
    reference: chr 0
allele count: 3
allele frequency: 3.603646890653341e-5
allele num: 83249
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1449G>A
  hgvsp: ENST00000541735.1:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8829G>A
  hgvsp: ENST00000357033.4:c.8829G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1449G>A
  hgvsp: ENST00000474231.1:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1449G>A
  hgvsp: ENST00000359836.1:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8817G>A
  hgvsp: ENST00000378677.2:c.8817G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1449G>A
  hgvsp: ENST00000378707.3:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1449G>A
  hgvsp: ENST00000343523.2:c.1449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1917G>A
  hgvsp: ENST00000358062.2:c.1917G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4956
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr2943Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

X-31496332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496332
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496332
    reference: chr 0
allele count: 3
allele frequency: 3.59277134405576e-5
allele num: 83501
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1448C>T
  hgvsp: ENSP00000444119.1:p.Thr483Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1448C>T
  hgvsp: ENSP00000417123.1:p.Thr483Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1448C>T
  hgvsp: ENSP00000367979.3:p.Thr483Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1916C>T
  hgvsp: ENSP00000350765.2:p.Thr639Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1448C>T
  hgvsp: ENSP00000340057.2:p.Thr483Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8828C>T
  hgvsp: ENSP00000354923.3:p.Thr2943Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8816C>T
  hgvsp: ENSP00000367948.2:p.Thr2939Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1448C>T
  hgvsp: ENSP00000352894.1:p.Thr483Met
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26654
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6267
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Thr2943Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-31496336-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496336
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496336
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 83979
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8812G>T
  hgvsp: ENSP00000367948.2:p.Ala2938Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1444G>T
  hgvsp: ENSP00000444119.1:p.Ala482Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1912G>T
  hgvsp: ENSP00000350765.2:p.Ala638Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1444G>T
  hgvsp: ENSP00000340057.2:p.Ala482Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8824G>T
  hgvsp: ENSP00000354923.3:p.Ala2942Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1444G>T
  hgvsp: ENSP00000367979.3:p.Ala482Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1444G>T
  hgvsp: ENSP00000352894.1:p.Ala482Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1444G>T
  hgvsp: ENSP00000417123.1:p.Ala482Ser
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13134
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4985
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29180
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala2942Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

X-31496349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496349
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496349
    reference: chr 0
allele count: 1
allele frequency: 1.177121467164197e-5
allele num: 84953
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8799G>A
  hgvsp: ENST00000378677.2:c.8799G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1899G>A
  hgvsp: ENST00000358062.2:c.1899G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1431G>A
  hgvsp: ENST00000474231.1:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1431G>A
  hgvsp: ENST00000541735.1:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8811G>A
  hgvsp: ENST00000357033.4:c.8811G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1431G>A
  hgvsp: ENST00000359836.1:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1431G>A
  hgvsp: ENST00000343523.2:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1431G>A
  hgvsp: ENST00000378707.3:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30047
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg2937Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-31496350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496350
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496350
    reference: chr 0
allele count: 78764
allele frequency: 9.045223822320219e-1
allele num: 87078
alternate allele: T
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8810G>A
  hgvsp: ENSP00000354923.3:p.Arg2937Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1430G>A
  hgvsp: ENSP00000352894.1:p.Arg477Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1430G>A
  hgvsp: ENSP00000444119.1:p.Arg477Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8798G>A
  hgvsp: ENSP00000367948.2:p.Arg2933Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1430G>A
  hgvsp: ENSP00000367979.3:p.Arg477Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1430G>A
  hgvsp: ENSP00000340057.2:p.Arg477Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1898G>A
  hgvsp: ENSP00000350765.2:p.Arg633Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1430G>A
  hgvsp: ENSP00000417123.1:p.Arg477Gln
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 9.75e1
  variant carriers: 5851
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 7.75e1
  variant carriers: 1297
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 7.25e1
  variant carriers: 1741
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.75e1
  variant carriers: 4519
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 3.25e1
  variant carriers: 5640
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 3032
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.25e1
  variant carriers: 980
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.75e1
  variant carriers: 3181
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 5.25e1
  variant carriers: 3491
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 2.75e1
  variant carriers: 6244
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.25e1
  variant carriers: 776
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 8.75e1
  variant carriers: 921
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.25e1
  variant carriers: 2726
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 2.25e1
  variant carriers: 5285
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 4.75e1
  variant carriers: 3648
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 4.25e1
  variant carriers: 3861
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 6.75e1
  variant carriers: 2158
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 1036
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.25e1
  variant carriers: 384
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 8.75e1
  variant carriers: 1211
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 126
hgvs: p.Arg2937Gln
num of homozygotes: 22571
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

X-31496352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496352
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496352
    reference: chr 0
allele count: 1
allele frequency: 1.145645972481584e-5
allele num: 87287
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1428C>T
  hgvsp: ENST00000541735.1:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8808C>T
  hgvsp: ENST00000357033.4:c.8808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1428C>T
  hgvsp: ENST00000343523.2:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1896C>T
  hgvsp: ENST00000358062.2:c.1896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1428C>T
  hgvsp: ENST00000378707.3:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1428C>T
  hgvsp: ENST00000359836.1:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1428C>T
  hgvsp: ENST00000474231.1:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8796C>T
  hgvsp: ENST00000378677.2:c.8796C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu2936Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-31496354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496354
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496354
    reference: chr 0
allele count: 1
allele frequency: 1.145501615157277e-5
allele num: 87298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1426C>T
  hgvsp: ENSP00000352894.1:p.Leu476Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1426C>T
  hgvsp: ENSP00000444119.1:p.Leu476Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1426C>T
  hgvsp: ENSP00000417123.1:p.Leu476Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1894C>T
  hgvsp: ENSP00000350765.2:p.Leu632Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1426C>T
  hgvsp: ENSP00000367979.3:p.Leu476Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8794C>T
  hgvsp: ENSP00000367948.2:p.Leu2932Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1426C>T
  hgvsp: ENSP00000340057.2:p.Leu476Phe
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8806C>T
  hgvsp: ENSP00000354923.3:p.Leu2936Phe
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu2936Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

X-31496381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496381
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496381
    reference: chr 0
allele count: 1
allele frequency: 1.143105360021033e-5
allele num: 87481
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1867A>G
  hgvsp: ENSP00000350765.2:p.Arg623Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1399A>G
  hgvsp: ENSP00000417123.1:p.Arg467Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8779A>G
  hgvsp: ENSP00000354923.3:p.Arg2927Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1399A>G
  hgvsp: ENSP00000352894.1:p.Arg467Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8767A>G
  hgvsp: ENSP00000367948.2:p.Arg2923Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1399A>G
  hgvsp: ENSP00000444119.1:p.Arg467Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1399A>G
  hgvsp: ENSP00000367979.3:p.Arg467Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1399A>G
  hgvsp: ENSP00000340057.2:p.Arg467Gly
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6099
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg2927Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

X-31496387-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496387
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496387
    reference: chr 0
allele count: 2
allele frequency: 2.285165845911267e-5
allele num: 87521
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1393T>C
  hgvsp: ENSP00000444119.1:p.Trp465Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1393T>C
  hgvsp: ENSP00000417123.1:p.Trp465Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8761T>C
  hgvsp: ENSP00000367948.2:p.Trp2921Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8773T>C
  hgvsp: ENSP00000354923.3:p.Trp2925Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1393T>C
  hgvsp: ENSP00000340057.2:p.Trp465Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1861T>C
  hgvsp: ENSP00000350765.2:p.Trp621Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1393T>C
  hgvsp: ENSP00000352894.1:p.Trp465Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1393T>C
  hgvsp: ENSP00000367979.3:p.Trp465Arg
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6187
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp2925Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-31496393-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496393
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496393
    reference: chr 0
allele count: 14
allele frequency: 1.599451616588598e-4
allele num: 87530
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8755G>T
  hgvsp: ENSP00000367948.2:p.Ala2919Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1387G>T
  hgvsp: ENSP00000352894.1:p.Ala463Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1387G>T
  hgvsp: ENSP00000417123.1:p.Ala463Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8767G>T
  hgvsp: ENSP00000354923.3:p.Ala2923Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1387G>T
  hgvsp: ENSP00000444119.1:p.Ala463Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1855G>T
  hgvsp: ENSP00000350765.2:p.Ala619Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1387G>T
  hgvsp: ENSP00000367979.3:p.Ala463Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1387G>T
  hgvsp: ENSP00000340057.2:p.Ala463Ser
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2690
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18385
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala2923Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

X-31496393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496393
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496393
    reference: chr 0
allele count: 1
allele frequency: 1.142465440420427e-5
allele num: 87530
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1387G>A
  hgvsp: ENSP00000367979.3:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1387G>A
  hgvsp: ENSP00000352894.1:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1387G>A
  hgvsp: ENSP00000340057.2:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1387G>A
  hgvsp: ENSP00000417123.1:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8755G>A
  hgvsp: ENSP00000367948.2:p.Ala2919Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1387G>A
  hgvsp: ENSP00000444119.1:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1855G>A
  hgvsp: ENSP00000350765.2:p.Ala619Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8767G>A
  hgvsp: ENSP00000354923.3:p.Ala2923Thr
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18385
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala2923Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

X-31496394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496394
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496394
    reference: chr 0
allele count: 1
allele frequency: 1.142113137727423e-5
allele num: 87557
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1386C>T
  hgvsp: ENST00000343523.2:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1386C>T
  hgvsp: ENST00000474231.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1386C>T
  hgvsp: ENST00000541735.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8754C>T
  hgvsp: ENST00000378677.2:c.8754C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1386C>T
  hgvsp: ENST00000378707.3:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8766C>T
  hgvsp: ENST00000357033.4:c.8766C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1386C>T
  hgvsp: ENST00000359836.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1854C>T
  hgvsp: ENST00000358062.2:c.1854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser2922Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

X-31496397-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496397
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496397
    reference: chr 0
allele count: 2
allele frequency: 2.283548177157668e-5
allele num: 87583
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8751C>T
  hgvsp: ENST00000378677.2:c.8751C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1851C>T
  hgvsp: ENST00000358062.2:c.1851C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1383C>T
  hgvsp: ENST00000378707.3:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1383C>T
  hgvsp: ENST00000541735.1:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1383C>T
  hgvsp: ENST00000474231.1:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8763C>T
  hgvsp: ENST00000357033.4:c.8763C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1383C>T
  hgvsp: ENST00000343523.2:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1383C>T
  hgvsp: ENST00000359836.1:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8801
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2715
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22257
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His2921His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

X-31496398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496398
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496398
    reference: chr 0
allele count: 2302
allele frequency: 2.629204500028554e-2
allele num: 87555
alternate allele: C
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8750A>G
  hgvsp: ENSP00000367948.2:p.His2917Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1382A>G
  hgvsp: ENSP00000340057.2:p.His461Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1850A>G
  hgvsp: ENSP00000350765.2:p.His617Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1382A>G
  hgvsp: ENSP00000417123.1:p.His461Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1382A>G
  hgvsp: ENSP00000352894.1:p.His461Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1382A>G
  hgvsp: ENSP00000444119.1:p.His461Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8762A>G
  hgvsp: ENSP00000354923.3:p.His2921Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1382A>G
  hgvsp: ENSP00000367979.3:p.His461Arg
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 7.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 3.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 5.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 9.75e1
  variant carriers: 555
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 6.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 3.75e1
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 5.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 8.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 6.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 2.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.75e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 10
hgvs: p.His2921Arg
num of homozygotes: 20
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

X-31496403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496403
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496403
    reference: chr 0
allele count: 13
allele frequency: 1.483984383918175e-4
allele num: 87602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1377C>T
  hgvsp: ENST00000343523.2:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1377C>T
  hgvsp: ENST00000378707.3:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1377C>T
  hgvsp: ENST00000541735.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8757C>T
  hgvsp: ENST00000357033.4:c.8757C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8745C>T
  hgvsp: ENST00000378677.2:c.8745C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1845C>T
  hgvsp: ENST00000358062.2:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1377C>T
  hgvsp: ENST00000359836.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1377C>T
  hgvsp: ENST00000474231.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn2919Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

X-31496407-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496407
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496407
    reference: chr 0
allele count: 1
allele frequency: 1.141304968100526e-5
allele num: 87619
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1373T>G
  hgvsp: ENSP00000340057.2:p.Leu458Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1841T>G
  hgvsp: ENSP00000350765.2:p.Leu614Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1373T>G
  hgvsp: ENSP00000417123.1:p.Leu458Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1373T>G
  hgvsp: ENSP00000367979.3:p.Leu458Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1373T>G
  hgvsp: ENSP00000444119.1:p.Leu458Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8753T>G
  hgvsp: ENSP00000354923.3:p.Leu2918Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8741T>G
  hgvsp: ENSP00000367948.2:p.Leu2914Trp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1373T>G
  hgvsp: ENSP00000352894.1:p.Leu458Trp
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu2918Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

X-31496415-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496415
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496415
    reference: chr 0
allele count: 1
allele frequency: 1.141265892127548e-5
allele num: 87622
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8745G>T
  hgvsp: ENSP00000354923.3:p.Trp2915Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1365G>T
  hgvsp: ENSP00000417123.1:p.Trp455Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1365G>T
  hgvsp: ENSP00000352894.1:p.Trp455Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1833G>T
  hgvsp: ENSP00000350765.2:p.Trp611Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1365G>T
  hgvsp: ENSP00000340057.2:p.Trp455Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8733G>T
  hgvsp: ENSP00000367948.2:p.Trp2911Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1365G>T
  hgvsp: ENSP00000367979.3:p.Trp455Cys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1365G>T
  hgvsp: ENSP00000444119.1:p.Trp455Cys
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Trp2915Cys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

X-31496418-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496418
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496418
    reference: chr 0
allele count: 1
allele frequency: 1.141226818830243e-5
allele num: 87625
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1362G>A
  hgvsp: ENST00000359836.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8730G>A
  hgvsp: ENST00000378677.2:c.8730G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1830G>A
  hgvsp: ENST00000358062.2:c.1830G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1362G>A
  hgvsp: ENST00000378707.3:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1362G>A
  hgvsp: ENST00000474231.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1362G>A
  hgvsp: ENST00000343523.2:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1362G>A
  hgvsp: ENST00000541735.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8742G>A
  hgvsp: ENST00000357033.4:c.8742G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu2914Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

X-31496419-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496419
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496419
    reference: chr 0
allele count: 1
allele frequency: 1.141239842965398e-5
allele num: 87624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1361A>T
  hgvsp: ENSP00000417123.1:p.Glu454Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8729A>T
  hgvsp: ENSP00000367948.2:p.Glu2910Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1829A>T
  hgvsp: ENSP00000350765.2:p.Glu610Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1361A>T
  hgvsp: ENSP00000352894.1:p.Glu454Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1361A>T
  hgvsp: ENSP00000367979.3:p.Glu454Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1361A>T
  hgvsp: ENSP00000444119.1:p.Glu454Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1361A>T
  hgvsp: ENSP00000340057.2:p.Glu454Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8741A>T
  hgvsp: ENSP00000354923.3:p.Glu2914Val
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19201
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu2914Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-31496426-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496426
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496426
    reference: chr 0
allele count: 1948
allele frequency: 2.223947392455932e-2
allele num: 87592
alternate allele: C
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1354A>G
  hgvsp: ENSP00000444119.1:p.Asn452Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1354A>G
  hgvsp: ENSP00000417123.1:p.Asn452Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1822A>G
  hgvsp: ENSP00000350765.2:p.Asn608Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1354A>G
  hgvsp: ENSP00000367979.3:p.Asn452Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1354A>G
  hgvsp: ENSP00000352894.1:p.Asn452Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1354A>G
  hgvsp: ENSP00000340057.2:p.Asn452Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8722A>G
  hgvsp: ENSP00000367948.2:p.Asn2908Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8734A>G
  hgvsp: ENSP00000354923.3:p.Asn2912Asp
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 6.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 5.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 4.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 8.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 9604
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 3.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 9.75e1
  variant carriers: 808
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 5.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 6.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 4.25e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 9.25e1
  variant carriers: 14
hgvs: p.Asn2912Asp
num of homozygotes: 27
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

X-31496431-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496431
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496431
    reference: chr 0
allele count: 1918
allele frequency: 2.19012275192692e-2
allele num: 87575
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1349A>T
  hgvsp: ENSP00000367979.3:p.Glu450Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1349A>T
  hgvsp: ENSP00000444119.1:p.Glu450Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8717A>T
  hgvsp: ENSP00000367948.2:p.Glu2906Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1349A>T
  hgvsp: ENSP00000352894.1:p.Glu450Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1349A>T
  hgvsp: ENSP00000340057.2:p.Glu450Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8729A>T
  hgvsp: ENSP00000354923.3:p.Glu2910Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1817A>T
  hgvsp: ENSP00000350765.2:p.Glu606Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign&pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1349A>T
  hgvsp: ENSP00000417123.1:p.Glu450Val
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 4.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 5.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 8.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 5.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 4.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 849
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 6.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 6306
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 6
hgvs: p.Glu2910Val
num of homozygotes: 24
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

X-31496442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496442
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496442
    reference: chr 0
allele count: 1
allele frequency: 1.14195662848725e-5
allele num: 87569
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8718G>A
  hgvsp: ENST00000357033.4:c.8718G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1338G>A
  hgvsp: ENST00000474231.1:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1338G>A
  hgvsp: ENST00000541735.1:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1806G>A
  hgvsp: ENST00000358062.2:c.1806G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1338G>A
  hgvsp: ENST00000343523.2:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.775G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1338G>A
  hgvsp: ENST00000378707.3:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8706G>A
  hgvsp: ENST00000378677.2:c.8706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1338G>A
  hgvsp: ENST00000359836.1:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys2906Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

X-31496447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496447
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496447
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87535
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1801C>T
  hgvsp: ENSP00000350765.2:p.Arg601Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8713C>T
  hgvsp: ENSP00000354923.3:p.Arg2905Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1333C>T
  hgvsp: ENSP00000417123.1:p.Arg445Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1333C>T
  hgvsp: ENSP00000367979.3:p.Arg445Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.770C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1333C>T
  hgvsp: ENSP00000340057.2:p.Arg445Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1333C>T
  hgvsp: ENSP00000444119.1:p.Arg445Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8701C>T
  hgvsp: ENSP00000367948.2:p.Arg2901Ter
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1333C>T
  hgvsp: ENSP00000352894.1:p.Arg445Ter
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: stop gained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6427
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg2905Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

X-31496448-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496448
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496448
    reference: chr 0
allele count: 1
allele frequency: 1.142361031780484e-5
allele num: 87538
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8712A>G
  hgvsp: ENST00000357033.4:c.8712A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1332A>G
  hgvsp: ENST00000359836.1:c.1332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1332A>G
  hgvsp: ENST00000343523.2:c.1332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1800A>G
  hgvsp: ENST00000358062.2:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8700A>G
  hgvsp: ENST00000378677.2:c.8700A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1332A>G
  hgvsp: ENST00000474231.1:c.1332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1332A>G
  hgvsp: ENST00000541735.1:c.1332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1332A>G
  hgvsp: ENST00000378707.3:c.1332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.769A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21688
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu2904Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

X-31496455-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496455
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496455
    reference: chr 0
allele count: 3
allele frequency: 3.429276879815276e-5
allele num: 87482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1325G>A
  hgvsp: ENSP00000444119.1:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1325G>A
  hgvsp: ENSP00000367979.3:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1793G>A
  hgvsp: ENSP00000350765.2:p.Arg598Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8693G>A
  hgvsp: ENSP00000367948.2:p.Arg2898Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1325G>A
  hgvsp: ENSP00000352894.1:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1325G>A
  hgvsp: ENSP00000340057.2:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1325G>A
  hgvsp: ENSP00000417123.1:p.Arg442Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.762G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8705G>A
  hgvsp: ENSP00000354923.3:p.Arg2902Gln
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg2902Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS

X-31496463-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496463
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496463
    reference: chr 0
allele count: 1
allele frequency: 1.143942253795028e-5
allele num: 87417
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1317T>A
  hgvsp: ENSP00000340057.2:p.Asn439Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1317T>A
  hgvsp: ENSP00000352894.1:p.Asn439Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1317T>A
  hgvsp: ENSP00000444119.1:p.Asn439Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1785T>A
  hgvsp: ENSP00000350765.2:p.Asn595Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.754T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8697T>A
  hgvsp: ENSP00000354923.3:p.Asn2899Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1317T>A
  hgvsp: ENSP00000417123.1:p.Asn439Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8685T>A
  hgvsp: ENSP00000367948.2:p.Asn2895Lys
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1317T>A
  hgvsp: ENSP00000367979.3:p.Asn439Lys
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn2899Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD

X-31496478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496478
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87275
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1302G>A
  hgvsp: ENST00000474231.1:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1302G>A
  hgvsp: ENST00000359836.1:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8670G>A
  hgvsp: ENST00000378677.2:c.8670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1770G>A
  hgvsp: ENST00000358062.2:c.1770G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8682G>A
  hgvsp: ENST00000357033.4:c.8682G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1302G>A
  hgvsp: ENST00000343523.2:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1302G>A
  hgvsp: ENST00000541735.1:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1302G>A
  hgvsp: ENST00000378707.3:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.739G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu2894Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-31496483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496483
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496483
    reference: chr 0
allele count: 5
allele frequency: 5.732761585911165e-5
allele num: 87218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1765C>T
  hgvsp: ENSP00000350765.2:p.Pro589Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.734C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1297C>T
  hgvsp: ENSP00000444119.1:p.Pro433Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1297C>T
  hgvsp: ENSP00000340057.2:p.Pro433Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8677C>T
  hgvsp: ENSP00000354923.3:p.Pro2893Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1297C>T
  hgvsp: ENSP00000367979.3:p.Pro433Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8665C>T
  hgvsp: ENSP00000367948.2:p.Pro2889Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1297C>T
  hgvsp: ENSP00000352894.1:p.Pro433Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1297C>T
  hgvsp: ENSP00000417123.1:p.Pro433Ser
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro2893Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

X-31496484-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496484
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496484
    reference: chr 0
allele count: 3
allele frequency: 3.440051371433813e-5
allele num: 87208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1296T>C
  hgvsp: ENST00000343523.2:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8676T>C
  hgvsp: ENST00000357033.4:c.8676T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8664T>C
  hgvsp: ENST00000378677.2:c.8664T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.733T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1296T>C
  hgvsp: ENST00000359836.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1296T>C
  hgvsp: ENST00000474231.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1764T>C
  hgvsp: ENST00000358062.2:c.1764T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1296T>C
  hgvsp: ENST00000378707.3:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1296T>C
  hgvsp: ENST00000541735.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro2892Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

X-31496486-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496486
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496486
    reference: chr 0
allele count: 1
allele frequency: 1.147038919030523e-5
allele num: 87181
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1294C>T
  hgvsp: ENSP00000352894.1:p.Pro432Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1294C>T
  hgvsp: ENSP00000367979.3:p.Pro432Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1762C>T
  hgvsp: ENSP00000350765.2:p.Pro588Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1294C>T
  hgvsp: ENSP00000444119.1:p.Pro432Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8662C>T
  hgvsp: ENSP00000367948.2:p.Pro2888Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1294C>T
  hgvsp: ENSP00000417123.1:p.Pro432Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8674C>T
  hgvsp: ENSP00000354923.3:p.Pro2892Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1294C>T
  hgvsp: ENSP00000340057.2:p.Pro432Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.731C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro2892Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-31496490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496490
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496490
    reference: chr 0
allele count: 1
allele frequency: 1.148079263392345e-5
allele num: 87102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1290G>A
  hgvsp: ENST00000541735.1:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1290G>A
  hgvsp: ENST00000359836.1:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1290G>A
  hgvsp: ENST00000474231.1:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1290G>A
  hgvsp: ENST00000378707.3:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8670G>A
  hgvsp: ENST00000357033.4:c.8670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1758G>A
  hgvsp: ENST00000358062.2:c.1758G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8658G>A
  hgvsp: ENST00000378677.2:c.8658G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1290G>A
  hgvsp: ENST00000343523.2:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.727G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18894
  bin: 6.25e1
  variant carriers: 0
hgvs: c.8670G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

X-31496498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496498
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496498
    reference: chr 0
allele count: 1
allele frequency: 1.149597066228287e-5
allele num: 86987
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1289-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1289-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8657-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1757-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1289-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.726-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1289-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8669-7A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1289-7A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: c.8669-7A>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

X-31496504-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496504
    reference: chr 0
allele count: 1
allele frequency: 1.151357450434062e-5
allele num: 86854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.726-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1289-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8669-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1289-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1289-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1289-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1757-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1289-13A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8657-13A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

X-31496506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496506
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496506
    reference: chr 0
allele count: 2
allele frequency: 2.304041288419889e-5
allele num: 86804
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1289-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1757-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1289-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8669-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.726-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1289-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1289-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1289-15A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8657-15A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6245
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

X-31496520-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24031496520
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24031496520
    reference: chr 0
allele count: 1
allele frequency: 1.157983718748914e-5
allele num: 86357
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000444119
  ensembl transcript: ENST00000541735
  gene symbol: DMD
  hgvsc: ENST00000541735.1:c.1289-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.8669-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000417123
  ensembl transcript: ENST00000474231
  gene symbol: DMD
  hgvsc: ENST00000474231.1:c.1289-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367979
  ensembl transcript: ENST00000378707
  gene symbol: DMD
  hgvsc: ENST00000378707.3:c.1289-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000445312
  gene symbol: DMD
  hgvsc: ENST00000445312.1:n.726-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000350765
  ensembl transcript: ENST00000358062
  gene symbol: DMD
  hgvsc: ENST00000358062.2:c.1757-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000352894
  ensembl transcript: ENST00000359836
  gene symbol: DMD
  hgvsc: ENST00000359836.1:c.1289-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.8657-29C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000340057
  ensembl transcript: ENST00000343523
  gene symbol: DMD
  hgvsc: ENST00000343523.2:c.1289-29C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16306
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5981
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11906
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 27487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8483
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47639
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.565515142291889e-4
allele num: 6571
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9937
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

FS
type: SiteQuality
SIO_000300: 7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.026e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 1.606e1

DP
type: SiteQuality
SIO_000300: 2.042498e6

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27306
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9937
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.22667557336896e-4
allele num: 4491
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8481
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9233
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.199298717114242e-5
allele num: 47627
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.117e0

FS
type: SiteQuality
SIO_000300: 6.176e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.040476e6

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11900
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26508
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2169
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9923
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6563
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4480
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179662616491683e-4
allele num: 8477
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

QD
type: SiteQuality
SIO_000300: 2.139e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.176e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.029748e6

GenotypeQuality
all individuals: 11899
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 697
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.1041999831664e-5
allele num: 47524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9221
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4479
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6549
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.348e0

DP
type: SiteQuality
SIO_000300: 2.004156e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -6.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.438e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.808e1

MQ
type: SiteQuality
SIO_000300: 5.786e1

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5737
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084598698481562e-4
allele num: 9220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4477
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6545
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8467
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.104997263503557e-5
allele num: 47506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.636e0

QD
type: SiteQuality
SIO_000300: 1.772e1

MQ
type: SiteQuality
SIO_000300: 5.898e1

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

DP
type: SiteQuality
SIO_000300: 1.999361e6

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4471
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.531628120692296e-4
allele num: 6529
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8459
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47449
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.417e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.302e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.96e-1

DP
type: SiteQuality
SIO_000300: 1.966007e6

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.654e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

QD
type: SiteQuality
SIO_000300: 3.07e0

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: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9717
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.546790409899459e-4
allele num: 6465
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8419
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47103
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.894886e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 8.75e-1

FS
type: SiteQuality
SIO_000300: 1.981e0

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7239
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.821825469120058e-4
allele num: 5489
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.301744337412132e-4
allele num: 7682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.68867797703869e-5
allele num: 37193
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7564
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.283e0

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

FS
type: SiteQuality
SIO_000300: 7.201e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.089e1

DP
type: SiteQuality
SIO_000300: 1.09217e6

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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5507
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 485
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7583
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.379310344827586e-4
allele num: 7250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7709
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37382
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

FS
type: SiteQuality
SIO_000300: 1.639e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.116904e6

GenotypeQuality
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bin: 3.75e1
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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.307714763408614e-5
allele num: 37681
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5551
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7767
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 489
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.155653e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.753e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

QD
type: SiteQuality
SIO_000300: 1.503e1

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: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5543
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7345
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.287001287001287e-4
allele num: 7770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37715
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3221
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.160419e6

FS
type: SiteQuality
SIO_000300: 2.272e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.294e0

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: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38741
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3361
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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East Asian
type: Population
allele count: 1
allele frequency: 1.756543123133673e-4
allele num: 5693
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.899e0

QD
type: SiteQuality
SIO_000300: 8.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7777
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5693
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.581244676182855e-5
allele num: 38741
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3361
num of homozygotes: 0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQ
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.899e0

MQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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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

GenotypeQuality
all individuals: 1587
bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7801
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.316309069369488e-4
allele num: 7597
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 515
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38969
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3393
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5720
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

FS
type: SiteQuality
SIO_000300: 9.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.076e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

DP
type: SiteQuality
SIO_000300: 1.23778e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

QD
type: SiteQuality
SIO_000300: 9.06e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.745200698080279e-4
allele num: 5730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8013
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3393
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 39044
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.241232e6

QD
type: SiteQuality
SIO_000300: 1.425e1

BaseQRankSum
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SIO_000300: -1.059e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 720
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3469
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5829
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 529
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8135
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.261829652996846e-4
allele num: 7925
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.749e1

DP
type: SiteQuality
SIO_000300: 1.261499e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.561e0

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: 2

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: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5849
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.997001798920648e-5
allele num: 40024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3489
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

QD
type: SiteQuality
SIO_000300: 1.492e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.007e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 1.304e0

DP
type: SiteQuality
SIO_000300: 1.273168e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

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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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7999
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.220703125e-4
allele num: 8192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7763
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5871
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.471607890017931e-5
allele num: 40152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 529
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

QD
type: SiteQuality
SIO_000300: 1.751e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 1.277286e6

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.75e1
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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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: 1
allele frequency: 1.288161793121216e-4
allele num: 7763
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5871
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7999
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 529
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

QD
type: SiteQuality
SIO_000300: 1.751e1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.277286e6

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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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele count: 1
allele frequency: 1.275672917463962e-4
allele num: 7839
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3607
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40709
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8273
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 530
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East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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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BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

FS
type: SiteQuality
SIO_000300: 1.2664e1

DP
type: SiteQuality
SIO_000300: 1.289557e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 532
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.443374789258924e-5
allele num: 40927
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3659
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
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.863931515844257e-5
allele num: 41119
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.297639e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 2.193e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4812
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41369
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.265662574357676e-4
allele num: 7901
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5987
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8265
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 541
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.521e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

FS
type: SiteQuality
SIO_000300: 1.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 1.302063e6

QD
type: SiteQuality
SIO_000300: 1.033e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 355
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4299
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 541
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.623188405797101e-4
allele num: 8280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41317
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8355
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5982
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.304773e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.166e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 296
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3739
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41677
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.662786830728301e-4
allele num: 6014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8351
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 5.456e0

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 1.320417e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 18433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1934
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variant carriers: 0

GenotypeQuality
all individuals: 1547
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variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4827
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6005
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3745
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8379
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7935
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.790992933285423e-5
allele num: 41745
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.776e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.61e-1

DP
type: SiteQuality
SIO_000300: 1.323877e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 302
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4835
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 765
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2242
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variant carriers: 0

GenotypeQuality
all individuals: 12062
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.960159362549801e-4
allele num: 6024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3761
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41893
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8463
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 547
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 4.015e0

QD
type: SiteQuality
SIO_000300: 1.769e1

DP
type: SiteQuality
SIO_000300: 1.326033e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.146e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 1126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
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variant carriers: 0

GenotypeQuality
all individuals: 9652
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variant carriers: 0

GenotypeQuality
all individuals: 4859
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variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5263
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1712
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.303935121186987e-5
allele num: 43404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8663
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3935
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6159
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.148e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.391479e6

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 19962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
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variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1950
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variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4861
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1966
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3937
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43508
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.153934918070621e-4
allele num: 8666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8791
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.398148e6

QD
type: SiteQuality
SIO_000300: 1.14e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 994
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variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8101
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43663
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8703
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3962
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.400204012240735e-4
allele num: 8823
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 1.548e1

DP
type: SiteQuality
SIO_000300: 1.403883e6

FS
type: SiteQuality
SIO_000300: 4.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

GenotypeQuality
all individuals: 1348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21423
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variant carriers: 0

GenotypeQuality
all individuals: 2608
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variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
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variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8101
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.290268648512471e-5
allele num: 43663
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8703
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8823
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

DP
type: SiteQuality
SIO_000300: 1.403883e6

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.44e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.548e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeQuality
all individuals: 250
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5262
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8867
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.123879473552154e-5
allele num: 43841
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.437607425232039e-4
allele num: 8727
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3992
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

QD
type: SiteQuality
SIO_000300: 1.455e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.417741e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.115e0

FS
type: SiteQuality
SIO_000300: 2.487e0

GenotypeQuality
all individuals: 1083
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 772
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variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8883
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.274743522667819e-5
allele num: 43961
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6205
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8133
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.991265285749938e-4
allele num: 4007
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

DP
type: SiteQuality
SIO_000300: 1.422875e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
all individuals: 1029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4893
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variant carriers: 1

GenotypeQuality
all individuals: 5535
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44324
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.225039813793948e-4
allele num: 8163
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4043
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 585
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8779
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.036e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.438686e6

QD
type: SiteQuality
SIO_000300: 2.241e1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.175e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2000
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 678
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45073
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6305
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8891
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8215
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.093613298337708e-4
allele num: 9144
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 1.479604e6

VQSLOD
type: SiteQuality
SIO_000300: -1.586e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.585e0

QD
type: SiteQuality
SIO_000300: 2.911e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.19896208989357e-5
allele num: 45476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9241
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -1.117e0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 1.49998e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

FS
type: SiteQuality
SIO_000300: 2.616e0

QD
type: SiteQuality
SIO_000300: 1.418e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

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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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4203
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6341
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.115075825156111e-4
allele num: 8968
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.418672148990204e-4
allele num: 8269
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 597
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

FS
type: SiteQuality
SIO_000300: 7.461e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.641e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

DP
type: SiteQuality
SIO_000300: 1.510094e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4221
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45757
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.339269813000891e-4
allele num: 8984
num of homozygotes: 0

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

African
type: Population
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
allele num: 9305
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 597
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.158e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

DP
type: SiteQuality
SIO_000300: 1.516484e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

GenotypeQuality
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bin: 5.75e1
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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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 970
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4255
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6387
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9017
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.531125e6

FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.672e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 7.75e1
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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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5028
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8373
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6437
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.147028512538647e-5
allele num: 46576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9529
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4335
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.148e0

VQSLOD
type: SiteQuality
SIO_000300: -3.346e0

DP
type: SiteQuality
SIO_000300: 1.568403e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.39e1

GenotypeQuality
all individuals: 2563
bin: 8.25e1
variant carriers: 2454

GenotypeQuality
all individuals: 936
bin: 5.75e1
variant carriers: 860

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 44

GenotypeQuality
all individuals: 2550
bin: 7.75e1
variant carriers: 2368

GenotypeQuality
all individuals: 387
bin: 2.25e1
variant carriers: 123

GenotypeQuality
all individuals: 1050
bin: 4.75e1
variant carriers: 972

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 51

GenotypeQuality
all individuals: 2545
bin: 6.75e1
variant carriers: 2140

GenotypeQuality
all individuals: 1447
bin: 5.25e1
variant carriers: 1349

GenotypeQuality
all individuals: 592
bin: 3.75e1
variant carriers: 509

GenotypeQuality
all individuals: 3976
bin: 6.25e1
variant carriers: 1905

GenotypeQuality
all individuals: 2331
bin: 9.25e1
variant carriers: 2276

GenotypeQuality
all individuals: 1371
bin: 7.25e1
variant carriers: 1223

GenotypeQuality
all individuals: 38316
bin: 9.75e1
variant carriers: 38154

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 86

GenotypeQuality
all individuals: 380
bin: 3.25e1
variant carriers: 296

European (Finnish)
type: Population
allele count: 4233
allele frequency: 9.421322056532384e-1
allele num: 4493
num of homozygotes: 1073

Other
type: Population
allele count: 585
allele frequency: 9.300476947535771e-1
allele num: 629
num of homozygotes: 157

African
type: Population
allele count: 8407
allele frequency: 9.888261585509291e-1
allele num: 8502
num of homozygotes: 3238

European (Non-Finnish)
type: Population
allele count: 45168
allele frequency: 9.459267015706806e-1
allele num: 47750
num of homozygotes: 13029

Latino
type: Population
allele count: 7225
allele frequency: 7.877235063235936e-1
allele num: 9172
num of homozygotes: 2195

East Asian
type: Population
allele count: 6079
allele frequency: 9.234391614765305e-1
allele num: 6583
num of homozygotes: 1978

South Asian
type: Population
allele count: 7067
allele frequency: 7.103226454920093e-1
allele num: 9949
num of homozygotes: 901

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 4.623e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.104000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

QD
type: SiteQuality
SIO_000300: 3.311e1

FS
type: SiteQuality
SIO_000300: 1.137e0

DP
type: SiteQuality
SIO_000300: 3.088085e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

GenotypeQuality
all individuals: 514
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
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GenotypeQuality
all individuals: 1328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 388
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variant carriers: 0

GenotypeQuality
all individuals: 877
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variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22257
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GenotypeQuality
all individuals: 2638
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variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13611
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8497
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9255
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.090432092313481e-5
allele num: 47837
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.157e0

FS
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.429764e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.313e0

QD
type: SiteQuality
SIO_000300: 2.588e1

GenotypeQuality
all individuals: 642
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
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GenotypeQuality
all individuals: 13693
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 1391
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GenotypeQuality
all individuals: 3359
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GenotypeQuality
all individuals: 5837
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GenotypeQuality
all individuals: 1329
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variant carriers: 0

GenotypeQuality
all individuals: 22258
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variant carriers: 1

GenotypeQuality
all individuals: 1481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9959
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.090169930815375e-5
allele num: 47843
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9261
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -1.524e0

MQ
type: SiteQuality
SIO_000300: 5.447e1

VQSLOD
type: SiteQuality
SIO_000300: -3.174e-1

DP
type: SiteQuality
SIO_000300: 2.429799e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.55e-1

QD
type: SiteQuality
SIO_000300: 2.224e1

FS
type: SiteQuality
SIO_000300: 1.018e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.362e0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3363
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 217
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variant carriers: 0

GenotypeQuality
all individuals: 404
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variant carriers: 0

GenotypeQuality
all individuals: 17754
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variant carriers: 0

GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 2126
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variant carriers: 0

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 1482
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variant carriers: 0

GenotypeQuality
all individuals: 22258
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6605
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077702338614075e-4
allele num: 9279
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8501
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 4.793e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.39e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 2.457252e6

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

GenotypeQuality
all individuals: 2785
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18143
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 156
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GenotypeQuality
all individuals: 2702
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GenotypeQuality
all individuals: 3381
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GenotypeQuality
all individuals: 2136
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GenotypeQuality
all individuals: 1486
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GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 22260
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variant carriers: 2

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8503
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9277
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10071
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.027092477675193e-4
allele num: 6607
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47913
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.209e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e0

DP
type: SiteQuality
SIO_000300: 2.463674e6

FS
type: SiteQuality
SIO_000300: 8.731e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 216
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22259
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2781
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 154
bin: 4.75e1
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GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10073
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.529411764705882e-3
allele num: 8500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077121930202499e-4
allele num: 9284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

QD
type: SiteQuality
SIO_000300: 1.853e1

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

DP
type: SiteQuality
SIO_000300: 2.469451e6

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

FS
type: SiteQuality
SIO_000300: 1.123e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.193e-1

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2690
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
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GenotypeQuality
all individuals: 165
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GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 3.25e1
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GenotypeQuality
all individuals: 2131
bin: 9.25e1
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GenotypeQuality
all individuals: 3373
bin: 7.75e1
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GenotypeQuality
all individuals: 1487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22259
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086898451521349e-5
allele num: 47918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10073
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

FS
type: SiteQuality
SIO_000300: 1.123e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.193e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

QD
type: SiteQuality
SIO_000300: 1.853e1

DP
type: SiteQuality
SIO_000300: 2.469451e6

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.25e1
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6228
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 171
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GenotypeQuality
all individuals: 1491
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 2138
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GenotypeQuality
all individuals: 22252
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GenotypeQuality
all individuals: 266
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GenotypeQuality
all individuals: 2783
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18579
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47925
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.992e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.470253e6

QD
type: SiteQuality
SIO_000300: 1.515e1

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18730
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.152620815843289e-4
allele num: 9291
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6615
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8499
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47941
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10083
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.398e0

QD
type: SiteQuality
SIO_000300: 1.811e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.005e0

VQSLOD
type: SiteQuality
SIO_000300: -1.886e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.471646e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.062e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

GenotypeQuality
all individuals: 22888
bin: 9.75e1
variant carriers: 2014

GenotypeQuality
all individuals: 2726
bin: 8.25e1
variant carriers: 39

GenotypeQuality
all individuals: 18322
bin: 6.25e1
variant carriers: 22

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6140
bin: 6.75e1
variant carriers: 24

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1453
bin: 8.75e1
variant carriers: 26

GenotypeQuality
all individuals: 2662
bin: 7.25e1
variant carriers: 20

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 13

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 10

GenotypeQuality
all individuals: 3292
bin: 7.75e1
variant carriers: 23

GenotypeQuality
all individuals: 2093
bin: 9.25e1
variant carriers: 36

Latino
type: Population
allele count: 159
allele frequency: 1.711517761033369e-2
allele num: 9290
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1628
allele frequency: 3.397896142928702e-2
allele num: 47912
num of homozygotes: 16

African
type: Population
allele count: 37
allele frequency: 4.353453347452641e-3
allele num: 8499
num of homozygotes: 0

South Asian
type: Population
allele count: 267
allele frequency: 2.647758825862753e-2
allele num: 10084
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 184
allele frequency: 4.070796460176991e-2
allele num: 4520
num of homozygotes: 1

Other
type: Population
allele count: 27
allele frequency: 4.272151898734177e-2
allele num: 632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

DP
type: SiteQuality
SIO_000300: 2.521853e6

FS
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: 4.056e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

QD
type: SiteQuality
SIO_000300: 1.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.658e-1

GenotypeQuality
all individuals: 1491
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18992
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22023
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 62
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variant carriers: 1

GenotypeQuality
all individuals: 11
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variant carriers: 1

GenotypeQuality
all individuals: 204
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variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.089864262360052e-3
allele num: 10093
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47941
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.164556962025316e-3
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9293
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.126e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.397e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.654e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.549e1

DP
type: SiteQuality
SIO_000300: 2.463969e6

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.359999999999999e0

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

GenotypeQuality
all individuals: 194
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 19049
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variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22017
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47947
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6627
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8497
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075962986873252e-4
allele num: 9294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.584e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

FS
type: SiteQuality
SIO_000300: 6.521e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

DP
type: SiteQuality
SIO_000300: 2.464274e6

VQSLOD
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.98e1

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

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6380
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2785
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variant carriers: 0

GenotypeQuality
all individuals: 19149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22015
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2756
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47949
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.02e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.294e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 5.873e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

DP
type: SiteQuality
SIO_000300: 2.465512e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.03e-2

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6397
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22015
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10101
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.178689297501179e-4
allele num: 8484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47948
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 2.465764e6

FS
type: SiteQuality
SIO_000300: 2.678e0

QD
type: SiteQuality
SIO_000300: 1.277e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.172e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.42e-1

GenotypeQuality
all individuals: 3396
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22015
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1486
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.178828244724744e-4
allele num: 8483
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47947
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.72e-1

MQ
type: SiteQuality
SIO_000300: 5.717e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.154e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.213e0

VQSLOD
type: SiteQuality
SIO_000300: -2.4e0

DP
type: SiteQuality
SIO_000300: 2.465798e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 4.93e-1

QD
type: SiteQuality
SIO_000300: 1.643e1

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 196
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1461
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2719
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2708
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 19012
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 6316
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 22487
bin: 9.75e1
variant carriers: 1808

GenotypeQuality
all individuals: 3326
bin: 7.75e1
variant carriers: 13

South Asian
type: Population
allele count: 124
allele frequency: 1.227236737925574e-2
allele num: 10104
num of homozygotes: 1

Other
type: Population
allele count: 6
allele frequency: 9.49367088607595e-3
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 241
allele frequency: 2.591955259195526e-2
allele num: 9298
num of homozygotes: 4

African
type: Population
allele count: 647
allele frequency: 7.647754137115839e-2
allele num: 8460
num of homozygotes: 19

East Asian
type: Population
allele count: 305
allele frequency: 4.597527886644558e-2
allele num: 6634
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 560
allele frequency: 1.16817556009846e-2
allele num: 47938
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 65
allele frequency: 1.436146707909854e-2
allele num: 4526
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.81e-1

DP
type: SiteQuality
SIO_000300: 2.529743e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.032e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.471e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2718
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 22473
bin: 9.75e1
variant carriers: 1785

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 19048
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1461
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2709
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3321
bin: 7.75e1
variant carriers: 10

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2102
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 9

South Asian
type: Population
allele count: 124
allele frequency: 1.227358210432545e-2
allele num: 10103
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 65
allele frequency: 1.436146707909854e-2
allele num: 4526
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 7.911392405063292e-3
allele num: 632
num of homozygotes: 0

East Asian
type: Population
allele count: 302
allele frequency: 4.555052790346908e-2
allele num: 6630
num of homozygotes: 2

Latino
type: Population
allele count: 241
allele frequency: 2.592234053995913e-2
allele num: 9297
num of homozygotes: 4

African
type: Population
allele count: 620
allele frequency: 7.335541883577851e-2
allele num: 8452
num of homozygotes: 16

European (Non-Finnish)
type: Population
allele count: 561
allele frequency: 1.170334828413477e-2
allele num: 47935
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.793e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.583e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

DP
type: SiteQuality
SIO_000300: 2.532996e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 2.406e1

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21690
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10107
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.186098920649982e-4
allele num: 8431
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47933
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.362e0

FS
type: SiteQuality
SIO_000300: 1.0202e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.173e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.241e1

DP
type: SiteQuality
SIO_000300: 2.451308e6

GenotypeQuality
all individuals: 3392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21688
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 290
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

QD
type: SiteQuality
SIO_000300: 1.18e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 3.809e0

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

DP
type: SiteQuality
SIO_000300: 2.4509e6

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

GenotypeQuality
all individuals: 1500
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.188071759534276e-4
allele num: 8417
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10109
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47914
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.450583e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

QD
type: SiteQuality
SIO_000300: 2.798e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.452e-1

GenotypeQuality
all individuals: 351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 19400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21686
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10107
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.225459627996989e-4
allele num: 9301
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.256e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.449821e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 3.972e0

GenotypeQuality
all individuals: 19331
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2162
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21683
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.089558476293959e-5
allele num: 47857
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.46e-2

DP
type: SiteQuality
SIO_000300: 2.447833e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21677
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19166
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.444203e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.831e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

GenotypeQuality
all individuals: 19112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21680
bin: 9.75e1
variant carriers: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.047361695888058e-4
allele num: 47739
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8297
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10099
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.108e0

QD
type: SiteQuality
SIO_000300: 2.222e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.530000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.807e0

DP
type: SiteQuality
SIO_000300: 2.442556e6

FS
type: SiteQuality
SIO_000300: 1.144e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.91e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21675
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19035
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8291
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.22754168908015e-4
allele num: 9295
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.441669e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.64e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

FS
type: SiteQuality
SIO_000300: 1.115e0

QD
type: SiteQuality
SIO_000300: 1.725e1

VQSLOD
type: SiteQuality
SIO_000300: -1.949e-1

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21674
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8279
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508295625942685e-4
allele num: 6630
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.137e0

QD
type: SiteQuality
SIO_000300: 9.58e0

FS
type: SiteQuality
SIO_000300: 1.736e0

MQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.441057e6

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2738
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21673
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.076194575979337e-4
allele num: 9292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8253
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.438564e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-1

QD
type: SiteQuality
SIO_000300: 1.084e1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 6.077e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
all individuals: 2745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 148
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21671
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6309
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9291
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.218323586744639e-4
allele num: 8208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

FS
type: SiteQuality
SIO_000300: 9.77e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

DP
type: SiteQuality
SIO_000300: 2.434532e6

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18264
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21670
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8155
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.102739870050676e-5
allele num: 47557
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 3.257e1

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.428741e6

GenotypeQuality
all individuals: 21670
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2708
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18087
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077470100204719e-4
allele num: 9281
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.442e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 7.95e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

DP
type: SiteQuality
SIO_000300: 2.426362e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1