X-32591981-AAGCACAGCATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032591981
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032591970
    reference: chr 0
allele count: 1
allele frequency: 1.339889861053421e-5
allele num: 74633
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  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
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  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
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20177
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: AAGCACAGCATC
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

X-32591987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032591987
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032591987
    reference: chr 0
allele count: 2
allele frequency: 2.735828408842197e-5
allele num: 73104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-24T>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.1591-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356807T>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.1603-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209160T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-24T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208671T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.5e0
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genotype depth: GenotypeDepth
  all individuals: 420
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 2540
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 378
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5521
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-32591991-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032591991
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032591991
    reference: chr 0
allele count: 1
allele frequency: 1.383585145829874e-5
allele num: 72276
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.1603-28A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208675A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-28A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-28A>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.1591-28A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-28A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356811A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209164A>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18113
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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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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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 388
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

X-32591995-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032591995
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032591995
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 70931
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.1603-32G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209168G>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.1591-32G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356815G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-32G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-32G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208679G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-32G>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11478
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20360
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

X-32592003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032592003
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032592003
    reference: chr 0
allele count: 1
allele frequency: 1.475100306820864e-5
allele num: 67792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208687A>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.1603-40A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209176A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-40A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356823A>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.1591-40A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16922
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5646
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

X-32592004-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032592004
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032592004
    reference: chr 0
allele count: 1
allele frequency: 1.490024287395885e-5
allele num: 67113
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1591-41C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-41C>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-41C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-41C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209177C>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356824C>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.1603-41C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208688C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16627
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5665
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

X-32592012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032592012
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032592012
    reference: chr 0
allele count: 6
allele frequency: 9.494872768704899e-5
allele num: 63192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-49G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-49G>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.1603-49G>A
  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.1591-49G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-356832G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-208696G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-209185G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-49G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14312
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5774
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

X-32601778-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032601778
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032601778
    reference: chr 0
allele count: 2
allele frequency: 1.385041551246537e-3
allele num: 1444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-9815T>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.1603-9815T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-366598T>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.1591-9815T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-218462T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-9815T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263600
  ensembl transcript: ENST00000578518
  gene symbol: MIR3915
  hgvsc: ENST00000578518.1:n.92T>C
  variant of: http://identifiers.org/hgnc/38955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-9815T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-218951T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

X-32601787-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032601787
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032601787
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 1444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-218471G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-9824G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-9824G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-366607G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-9824G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-218960G>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.1603-9824G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263600
  ensembl transcript: ENST00000578518
  gene symbol: MIR3915
  hgvsc: ENST00000578518.1:n.83G>A
  variant of: http://identifiers.org/hgnc/38955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1591-9824G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

X-32601879-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032601879
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032601879
    reference: chr 0
allele count: 1
allele frequency: 6.939625260235947e-4
allele num: 1441
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-9916A>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.1591-9916A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-9916A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-218563A>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.1603-9916A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-366699A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-219052A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-9916A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

X-32601903-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032601903
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032601903
    reference: chr 0
allele count: 1
allele frequency: 6.939625260235947e-4
allele num: 1441
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-219076T>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.1591-9940T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-366723T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-218587T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-9940T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-9940T>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.1603-9940T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-9940T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

X-32601914-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032601914
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032601914
    reference: chr 0
allele count: 1
allele frequency: 6.939625260235947e-4
allele num: 1441
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1591-9951A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-9951A>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.1603-9951A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-366734A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1579-9951A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-218598A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-9951A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-219087A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-32613828-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613828
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613828
    reference: chr 0
allele count: 1
allele frequency: 1.376974236812029e-5
allele num: 72623
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231001C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230512C>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.1602+46C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21865C>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378648C>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.1590+46C>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21865C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+46C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 11651
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 5988
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genotype depth: GenotypeDepth
  all individuals: 386
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genotype depth: GenotypeDepth
  all individuals: 3329
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
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genotype quality: GenotypeQuality
  all individuals: 5497
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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: 8958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

X-32613831-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613831
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613830
    reference: chr 0
allele count: 1
allele frequency: 1.375042970092815e-5
allele num: 72725
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21869delA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231005delA
  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.1590+42delA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230516delA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21869delA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+42delA
  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.1602+42delA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378652delA
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: CT
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-32613832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613832
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613832
    reference: chr 0
allele count: 1
allele frequency: 1.373003995441627e-5
allele num: 72833
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21869A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21869A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378652A>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.1590+42A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+42A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230516A>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.1602+42A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231005A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3381
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 154
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15344
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9835
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genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6887
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5397
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

X-32613841-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613841
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613841
    reference: chr 0
allele count: 1
allele frequency: 1.354224503338163e-5
allele num: 73843
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1590+33T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+33T>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.1602+33T>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378661T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21878T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231014T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230525T>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21878T>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

X-32613843-ATATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613843
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613839
    reference: chr 0
allele count: 1
allele frequency: 1.348926928628276e-5
allele num: 74133
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21884_247-21881delAATA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  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.1602+27_1602+30delAATA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+27_1578+30delAATA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21884_87-21881delAATA
  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.1590+27_1590+30delAATA
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 337
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: ATATT
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

X-32613847-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613847
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613847
    reference: chr 0
allele count: 2
allele frequency: 2.677842194759463e-5
allele num: 74687
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378667A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231020A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+27A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21884A>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.1590+27A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21884A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230531A>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.1602+27A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21205
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
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genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
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genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10507
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 617
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6892
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-32613857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613857
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613857
    reference: chr 0
allele count: 2
allele frequency: 2.613183510812047e-5
allele num: 76535
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378677T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231030T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21894T>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.1590+17T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+17T>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.1602+17T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21894T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230541T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24760
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

X-32613861-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613861
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613861
    reference: chr 0
allele count: 3
allele frequency: 3.872366790582404e-5
allele num: 77472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+13T>A
  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.1590+13T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230545T>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.1602+13T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21898T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231034T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21898T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378681T>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6894
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-32613866-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613866
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613866
    reference: chr 0
allele count: 1
allele frequency: 1.275819395006443e-5
allele num: 78381
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231039T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1578+8T>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.1602+8T>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378686T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21903T>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.1590+8T>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21903T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230550T>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27271
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8470
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1602+8T>G
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-32613875-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613875
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613875
    reference: chr 0
allele count: 1
allele frequency: 1.248985199525386e-5
allele num: 80065
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230559A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231048A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1589A>T
  hgvsp: ENSP00000367948.2:p.Lys530Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21912A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1577A>T
  hgvsp: ENSP00000288447.4:p.Lys526Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.1601A>T
  hgvsp: ENSP00000354923.3:p.Lys534Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21912A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378695A>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29179
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7229
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys534Met
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-32613882-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613882
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613882
    reference: chr 0
allele count: 1
allele frequency: 1.234034676374406e-5
allele num: 81035
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21919C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1570C>G
  hgvsp: ENSP00000288447.4:p.Gln524Glu
  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.1594C>G
  hgvsp: ENSP00000354923.3:p.Gln532Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378702C>G
  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.1582C>G
  hgvsp: ENSP00000367948.2:p.Gln528Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231055C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230566C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21919C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33294
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6891
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln532Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

X-32613893-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613893
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613893
    reference: chr 0
allele count: 1
allele frequency: 1.217285453438831e-5
allele num: 82150
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.1583C>A
  hgvsp: ENSP00000354923.3:p.Ala528Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231066C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1559C>A
  hgvsp: ENSP00000288447.4:p.Ala520Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21930C>A
  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.1571C>A
  hgvsp: ENSP00000367948.2:p.Ala524Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378713C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230577C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21930C>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5703
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala528Asp
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

X-32613894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613894
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613894
    reference: chr 0
allele count: 5
allele frequency: 6.080284070871791e-5
allele num: 82233
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230578G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1558G>A
  hgvsp: ENSP00000288447.4:p.Ala520Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21931G>A
  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.1570G>A
  hgvsp: ENSP00000367948.2:p.Ala524Thr
  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.1582G>A
  hgvsp: ENSP00000354923.3:p.Ala528Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231067G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21931G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378714G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4129
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala528Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

X-32613896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613896
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613896
    reference: chr 0
allele count: 1
allele frequency: 1.213312464358946e-5
allele num: 82419
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.1568C>T
  hgvsp: ENSP00000367948.2:p.Ala523Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230580C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1556C>T
  hgvsp: ENSP00000288447.4:p.Ala519Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21933C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378716C>T
  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.1580C>T
  hgvsp: ENSP00000354923.3:p.Ala527Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21933C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231069C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala527Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

X-32613901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613901
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613901
    reference: chr 0
allele count: 6
allele frequency: 7.24839025333124e-5
allele num: 82777
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231074A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21938A>G
  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.1563A>G
  hgvsp: ENST00000378677.2:c.1563A>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.1575A>G
  hgvsp: ENST00000357033.4:c.1575A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378721A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21938A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1551A>G
  hgvsp: ENST00000288447.4:c.1551A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230585A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6896
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala525Ala
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

X-32613903-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613903
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613903
    reference: chr 0
allele count: 1
allele frequency: 1.207088020858481e-5
allele num: 82844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231076G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21940G>A
  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.1561G>A
  hgvsp: ENSP00000367948.2:p.Ala521Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378723G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230587G>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.1573G>A
  hgvsp: ENSP00000354923.3:p.Ala525Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1549G>A
  hgvsp: ENSP00000288447.4:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21940G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala525Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

X-32613904-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613904
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613904
    reference: chr 0
allele count: 1
allele frequency: 1.205574576843323e-5
allele num: 82948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1560C>A
  hgvsp: ENSP00000367948.2:p.His520Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378724C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21941C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230588C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1548C>A
  hgvsp: ENSP00000288447.4:p.His516Gln
  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.1572C>A
  hgvsp: ENSP00000354923.3:p.His524Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231077C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21941C>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6893
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5081
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His524Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

X-32613908-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613908
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613908
    reference: chr 0
allele count: 1
allele frequency: 1.202038657563227e-5
allele num: 83192
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.1556A>T
  hgvsp: ENSP00000367948.2:p.Asp519Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1544A>T
  hgvsp: ENSP00000288447.4:p.Asp515Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378728A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231081A>T
  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.1568A>T
  hgvsp: ENSP00000354923.3:p.Asp523Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230592A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21945A>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21945A>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp523Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

X-32613909-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613909
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613909
    reference: chr 0
allele count: 1
allele frequency: 1.201388805459111e-5
allele num: 83237
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1543G>C
  hgvsp: ENSP00000288447.4:p.Asp515His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21946G>C
  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.1567G>C
  hgvsp: ENSP00000354923.3:p.Asp523His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230593G>C
  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.1555G>C
  hgvsp: ENSP00000367948.2:p.Asp519His
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21946G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231082G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378729G>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp523His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

X-32613912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613912
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613912
    reference: chr 0
allele count: 1
allele frequency: 1.199731260197716e-5
allele num: 83352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1552G>A
  hgvsp: ENSP00000367948.2:p.Gly518Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378732G>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.1564G>A
  hgvsp: ENSP00000354923.3:p.Gly522Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1540G>A
  hgvsp: ENSP00000288447.4:p.Gly514Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21949G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230596G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231085G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21949G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4251
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly522Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-32613919-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613919
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613919
    reference: chr 0
allele count: 1
allele frequency: 1.194857334034316e-5
allele num: 83692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1533A>C
  hgvsp: ENSP00000288447.4:p.Glu511Asp
  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.1557A>C
  hgvsp: ENSP00000354923.3:p.Glu519Asp
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21956A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230603A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378739A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21956A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231092A>C
  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.1545A>C
  hgvsp: ENSP00000367948.2:p.Glu515Asp
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu519Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

X-32613922-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613922
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613922
    reference: chr 0
allele count: 319
allele frequency: 3.806410042240412e-3
allele num: 83806
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230606T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21959T>A
  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.1542T>A
  hgvsp: ENSP00000367948.2:p.Asp514Glu
  variant of: http://identifiers.org/hgnc/2928
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.1554T>A
  hgvsp: ENSP00000354923.3:p.Asp518Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231095T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1530T>A
  hgvsp: ENSP00000288447.4:p.Asp510Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21959T>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378742T>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 30817
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10408
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 5.25e1
  variant carriers: 3
hgvs: p.Asp518Glu
num of homozygotes: 6
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

X-32613928-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613928
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613928
    reference: chr 0
allele count: 1
allele frequency: 1.188919272381405e-5
allele num: 84110
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.1548A>C
  hgvsp: ENST00000357033.4:c.1548A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21965A>C
  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.1536A>C
  hgvsp: ENST00000378677.2:c.1536A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231101A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1524A>C
  hgvsp: ENST00000288447.4:c.1524A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21965A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230612A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378748A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4232
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6898
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val516Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

X-32613931-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613931
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613931
    reference: chr 0
allele count: 1
allele frequency: 1.187718985687986e-5
allele num: 84195
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230615G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21968G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1521G>T
  hgvsp: ENST00000288447.4:c.1521G>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.1545G>T
  hgvsp: ENST00000357033.4:c.1545G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378751G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21968G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231104G>T
  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.1533G>T
  hgvsp: ENST00000378677.2:c.1533G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val515Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

X-32613931-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613931
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613931
    reference: chr 0
allele count: 1
allele frequency: 1.187718985687986e-5
allele num: 84195
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1533G>C
  hgvsp: ENST00000378677.2:c.1533G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378751G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21968G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230615G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21968G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1521G>C
  hgvsp: ENST00000288447.4:c.1521G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231104G>C
  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.1545G>C
  hgvsp: ENST00000357033.4:c.1545G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6899
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val515Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

X-32613932-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613932
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613932
    reference: chr 0
allele count: 1
allele frequency: 1.186661920018987e-5
allele num: 84270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231105T>C
  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.1532T>C
  hgvsp: ENSP00000367948.2:p.Val511Ala
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1520T>C
  hgvsp: ENSP00000288447.4:p.Val507Ala
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21969T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21969T>C
  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.1544T>C
  hgvsp: ENSP00000354923.3:p.Val515Ala
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230616T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378752T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val515Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

X-32613934-C-CACCATGTGAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613934
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613944
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 84353
alternate allele: CACCATGTGAG
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsp: ENSP00000354923.3:p.Val515SerfsTer7
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsp: ENSP00000367948.2:p.Val511SerfsTer7
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsp: ENSP00000288447.4:p.Val507SerfsTer7
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31350
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6900
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val515SerfsTer7
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

X-32613939-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613939
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613939
    reference: chr 0
allele count: 1
allele frequency: 1.183515989301015e-5
allele num: 84494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21976A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230623A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378759A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231112A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1513A>G
  hgvsp: ENSP00000288447.4:p.Met505Val
  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.1525A>G
  hgvsp: ENSP00000367948.2:p.Met509Val
  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.1537A>G
  hgvsp: ENSP00000354923.3:p.Met513Val
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21976A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6900
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met513Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-32613939-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613939
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613939
    reference: chr 0
allele count: 1
allele frequency: 1.183515989301015e-5
allele num: 84494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1513A>C
  hgvsp: ENSP00000288447.4:p.Met505Leu
  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.1537A>C
  hgvsp: ENSP00000354923.3:p.Met513Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231112A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230623A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378759A>C
  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.1525A>C
  hgvsp: ENSP00000367948.2:p.Met509Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21976A>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21976A>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36815
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met513Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-32613940-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613940
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613940
    reference: chr 0
allele count: 1
allele frequency: 1.183698109634119e-5
allele num: 84481
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231113C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21977C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230624C>T
  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.1536C>T
  hgvsp: ENST00000357033.4:c.1536C>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.1524C>T
  hgvsp: ENST00000378677.2:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378760C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1512C>T
  hgvsp: ENST00000288447.4:c.1512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21977C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His512His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-32613940-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613940
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613940
    reference: chr 0
allele count: 1
allele frequency: 1.183698109634119e-5
allele num: 84481
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231113C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21977C>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.1536C>A
  hgvsp: ENSP00000354923.3:p.His512Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378760C>A
  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.1524C>A
  hgvsp: ENSP00000367948.2:p.His508Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1512C>A
  hgvsp: ENSP00000288447.4:p.His504Gln
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230624C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21977C>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His512Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

X-32613942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613942
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613942
    reference: chr 0
allele count: 1
allele frequency: 1.182802058075581e-5
allele num: 84545
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.1522C>T
  hgvsp: ENSP00000367948.2:p.His508Tyr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378762C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230626C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21979C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21979C>T
  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.1534C>T
  hgvsp: ENSP00000354923.3:p.His512Tyr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1510C>T
  hgvsp: ENSP00000288447.4:p.His504Tyr
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231115C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6897
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His512Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-32613955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613955
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613955
    reference: chr 0
allele count: 1
allele frequency: 1.182144883676944e-5
allele num: 84592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230639C>T
  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.1509C>T
  hgvsp: ENST00000378677.2:c.1509C>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.1521C>T
  hgvsp: ENST00000357033.4:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21992C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378775C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1497C>T
  hgvsp: ENST00000288447.4:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231128C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21992C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val507Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-32613958-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613958
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613958
    reference: chr 0
allele count: 3
allele frequency: 3.548951876212559e-5
allele num: 84532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-21995G>T
  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.1506G>T
  hgvsp: ENSP00000367948.2:p.Arg502Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1494G>T
  hgvsp: ENSP00000288447.4:p.Arg498Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231131G>T
  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.1518G>T
  hgvsp: ENSP00000354923.3:p.Arg506Ser
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378778G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-21995G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230642G>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Arg506Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

X-32613963-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613963
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613963
    reference: chr 0
allele count: 99
allele frequency: 1.174432950555186e-3
allele num: 84296
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22000G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230647G>C
  variant of: http://identifiers.org/hgnc/2928
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.1513G>C
  hgvsp: ENSP00000354923.3:p.Val505Leu
  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.1501G>C
  hgvsp: ENSP00000367948.2:p.Val501Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22000G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231136G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378783G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1489G>C
  hgvsp: ENSP00000288447.4:p.Val497Leu
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30105
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4342
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.75e1
  variant carriers: 2
hgvs: p.Val505Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-32613967-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613967
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613967
    reference: chr 0
allele count: 1
allele frequency: 1.185705138846072e-5
allele num: 84338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1485A>G
  hgvsp: ENST00000288447.4:c.1485A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22004A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378787A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230651A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22004A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231140A>G
  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.1497A>G
  hgvsp: ENST00000378677.2:c.1497A>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.1509A>G
  hgvsp: ENST00000357033.4:c.1509A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6895
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu503Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-32613973-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613973
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613973
    reference: chr 0
allele count: 7
allele frequency: 8.344061412291994e-5
allele num: 83892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1479A>G
  hgvsp: ENST00000288447.4:c.1479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230657A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378793A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22010A>G
  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.1491A>G
  hgvsp: ENST00000378677.2:c.1491A>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.1503A>G
  hgvsp: ENST00000357033.4:c.1503A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22010A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231146A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Glu501Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

X-32613983-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613983
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613983
    reference: chr 0
allele count: 1
allele frequency: 1.199889610155866e-5
allele num: 83341
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230667A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1469A>G
  hgvsp: ENSP00000288447.4:p.Glu490Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22020A>G
  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.1481A>G
  hgvsp: ENSP00000367948.2:p.Glu494Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231156A>G
  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.1493A>G
  hgvsp: ENSP00000354923.3:p.Glu498Gly
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378803A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22020A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6895
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6824
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34215
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu498Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

X-32613993-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613993
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613993
    reference: chr 0
allele count: 2
allele frequency: 2.430694814112614e-5
allele num: 82281
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22030G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1471G>T
  hgvsp: ENSP00000367948.2:p.Val491Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.1483G>T
  hgvsp: ENSP00000354923.3:p.Val495Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22030G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231166G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459G>T
  hgvsp: ENSP00000288447.4:p.Val487Leu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230677G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378813G>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6896
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Val495Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

X-32613993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032613993
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032613993
    reference: chr 0
allele count: 1
allele frequency: 1.215347407056307e-5
allele num: 82281
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378813G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230677G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1471G>A
  hgvsp: ENSP00000367948.2:p.Val491Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459G>A
  hgvsp: ENSP00000288447.4:p.Val487Met
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22030G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22030G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231166G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.1483G>A
  hgvsp: ENSP00000354923.3:p.Val495Met
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6896
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8888
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31091
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val495Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

X-32614000-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032614000
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032614000
    reference: chr 0
allele count: 52
allele frequency: 6.389069776013957e-4
allele num: 81389
alternate allele: C
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000354923
  ensembl transcript: ENST00000357033
  gene symbol: DMD
  hgvsc: ENST00000357033.4:c.1483-7C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378820C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22037C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231173C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230684C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22037C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1471-7C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459-7C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22387
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10638
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27927
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1483-7C>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

X-32614029-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032614029
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032614029
    reference: chr 0
allele count: 3
allele frequency: 3.855892446306698e-5
allele num: 77803
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22066T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231202T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378849T>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.1483-36T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459-36T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22066T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230713T>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.1471-36T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

X-32614034-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032614034
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032614034
    reference: chr 0
allele count: 1
allele frequency: 1.297286077525816e-5
allele num: 77084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22071G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378854G>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.1483-41G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231207G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230718G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22071G>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459-41G>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.1471-41G>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5817
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10749
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-32614036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032614036
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032614036
    reference: chr 0
allele count: 1
allele frequency: 1.303967974546545e-5
allele num: 76689
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459-43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230720A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22073A>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.1483-43A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22073A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231209A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378856A>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.1471-43A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9030
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5887
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1100
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10671
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3803
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

X-32614038-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032614038
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032614036
    reference: chr 0
allele count: 1
allele frequency: 1.309260398800718e-5
allele num: 76379
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-22077_247-22076delAT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-230724_94-230723delAT
  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.1471-47_1471-46delAT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1459-47_1459-46delAT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-22077_87-22076delAT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-378860_336-378859delAT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-231213_94-231212delAT
  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.1483-47_1483-46delAT
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3781
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CAT
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

X-32632372-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632372
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632372
    reference: chr 0
allele count: 1
allele frequency: 1.17262163017859e-5
allele num: 85279
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.1482+48T>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.1470+48T>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397192T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40409T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+48T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249056T>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40409T>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249545T>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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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
  all individuals: 323
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genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 251
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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: 187
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2216
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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: 301
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genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-32632383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632383
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632383
    reference: chr 0
allele count: 2
allele frequency: 2.343704224526865e-5
allele num: 85335
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40420A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40420A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+37A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397203A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249067A>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.1482+37A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249556A>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.1470+37A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  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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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: 446
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 176
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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: 1307
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genotype quality: GenotypeQuality
  all individuals: 393
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-32632388-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632388
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632388
    reference: chr 0
allele count: 5
allele frequency: 5.856652571656144e-5
allele num: 85373
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+32T>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.1470+32T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249072T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249561T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397208T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40425T>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.1482+32T>C
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40425T>C
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
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  variant carriers: 1
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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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

X-32632399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632399
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632399
    reference: chr 0
allele count: 8
allele frequency: 9.343393053187265e-5
allele num: 85622
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.1470+21G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249572G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+21G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397219G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40436G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40436G>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.1482+21G>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249083G>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
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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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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4188
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

X-32632401-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632401
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632401
    reference: chr 0
allele count: 1
allele frequency: 1.166507244009985e-5
allele num: 85726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1470+19G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249085G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40438G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+19G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397221G>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.1482+19G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40438G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249574G>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 249
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25897
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
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genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
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genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 215
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

X-32632409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632409
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632409
    reference: chr 0
allele count: 2
allele frequency: 2.323771015604122e-5
allele num: 86067
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249093C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+11C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40446C>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.1482+11C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40446C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397229C>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.1470+11C>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249582C>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
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genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 511
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
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genotype quality: GenotypeQuality
  all individuals: 821
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genotype quality: GenotypeQuality
  all individuals: 5549
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-32632409-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632409
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632409
    reference: chr 0
allele count: 3
allele frequency: 3.485656523406183e-5
allele num: 86067
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.1470+11C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397229C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40446C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+11C>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.1482+11C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40446C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249582C>A
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249093C>A
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
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genotype depth: GenotypeDepth
  all individuals: 660
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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: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27518
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 4268
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genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 491
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 284
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 165
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genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-32632411-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632412
    reference: chr 0
allele count: 1
allele frequency: 1.16048322521498e-5
allele num: 86171
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+8dupT
  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.1482+8dupT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40449dupT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249585dupT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397232dupT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249096dupT
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40449dupT
  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.1470+8dupT
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5594
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

X-32632413-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632413
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632413
    reference: chr 0
allele count: 3
allele frequency: 3.48052068589461e-5
allele num: 86194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40450G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249097G>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.1470+7G>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.1482+7G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249586G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+7G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40450G>T
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397233G>T
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
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genotype depth: GenotypeDepth
  all individuals: 324
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genotype depth: GenotypeDepth
  all individuals: 208
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
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genotype depth: GenotypeDepth
  all individuals: 1146
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genotype depth: GenotypeDepth
  all individuals: 1261
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genotype depth: GenotypeDepth
  all individuals: 517
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genotype depth: GenotypeDepth
  all individuals: 163
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genotype depth: GenotypeDepth
  all individuals: 442
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genotype depth: GenotypeDepth
  all individuals: 134
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genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 824
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genotype quality: GenotypeQuality
  all individuals: 40
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genotype quality: GenotypeQuality
  all individuals: 518
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genotype quality: GenotypeQuality
  all individuals: 435
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genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1482+7G>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum

X-32632417-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632417
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632417
    reference: chr 0
allele count: 1
allele frequency: 1.157796019497285e-5
allele num: 86371
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397237A>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.1470+3A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249101A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1458+3A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249590A>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.1482+3A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40454A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40454A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
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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
  all individuals: 208
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43428
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genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1482+3A>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-32632429-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632429
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632429
    reference: chr 0
allele count: 1
allele frequency: 1.154108047595416e-5
allele num: 86647
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249113A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249602A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397249A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40466A>G
  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.1461A>G
  hgvsp: ENST00000378677.2:c.1461A>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.1473A>G
  hgvsp: ENST00000357033.4:c.1473A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1449A>G
  hgvsp: ENST00000288447.4:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40466A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln491Gln
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

X-32632430-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632430
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632430
    reference: chr 0
allele count: 1
allele frequency: 1.153748528970626e-5
allele num: 86674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000367948
  ensembl transcript: ENST00000378677
  gene symbol: DMD
  hgvsc: ENST00000378677.2:c.1460A>G
  hgvsp: ENSP00000367948.2:p.Gln487Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397250A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249114A>G
  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.1472A>G
  hgvsp: ENSP00000354923.3:p.Gln491Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249603A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1448A>G
  hgvsp: ENSP00000288447.4:p.Gln483Arg
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40467A>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: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40467A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4183
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln491Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff

X-32632431-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632431
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632431
    reference: chr 0
allele count: 1
allele frequency: 1.153761840480888e-5
allele num: 86673
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40468C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249115C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40468C>G
  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.1471C>G
  hgvsp: ENSP00000354923.3:p.Gln491Glu
  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.1459C>G
  hgvsp: ENSP00000367948.2:p.Gln487Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397251C>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1447C>G
  hgvsp: ENSP00000288447.4:p.Gln483Glu
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249604C>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln491Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

X-32632432-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24032632432
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24032632432
    reference: chr 0
allele count: 1
allele frequency: 1.153482363254666e-5
allele num: 86694
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.1470A>G
  hgvsp: ENST00000357033.4:c.1470A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl transcript: ENST00000480751
  gene symbol: DMD
  hgvsc: ENST00000480751.1:n.87-40469A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000288447
  ensembl transcript: ENST00000288447
  gene symbol: DMD
  hgvsc: ENST00000288447.4:c.1446A>G
  hgvsp: ENST00000288447.4:c.1446A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000399897
  ensembl transcript: ENST00000420596
  gene symbol: DMD
  hgvsc: ENST00000420596.1:c.94-249116A>G
  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.1458A>G
  hgvsp: ENST00000378677.2:c.1458A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000388559
  ensembl transcript: ENST00000448370
  gene symbol: DMD
  hgvsc: ENST00000448370.1:c.94-249605A>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: ENST00000488902
  gene symbol: DMD
  hgvsc: ENST00000488902.1:n.336-397252A>G
  variant of: http://identifiers.org/hgnc/2928
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198947
  ensembl protein: ENSP00000395904
  ensembl transcript: ENST00000447523
  gene symbol: DMD
  hgvsc: ENST00000447523.1:c.247-40469A>G
  variant of: http://identifiers.org/hgnc/2928
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val490Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T

GenotypeQuality
all individuals: 1061
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 422
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3290
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.205690860863275e-4
allele num: 8294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40407
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7765
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3703
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.122e1

MQ
type: SiteQuality
SIO_000300: 4.012e1

DP
type: SiteQuality
SIO_000300: 1.361394e6

GenotypeQuality
all individuals: 111
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20863
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7857
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5799
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.449479485609308e-4
allele num: 8165
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 523
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.309e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

DP
type: SiteQuality
SIO_000300: 1.297098e6

QD
type: SiteQuality
SIO_000300: 2.574e1

GenotypeQuality
all individuals: 2670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3628
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5518
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5713
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.564760194921775e-5
allele num: 38990
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.32e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.651e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.639e0

MQRankSum
type: SiteQuality
SIO_000300: -2.361e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

DP
type: SiteQuality
SIO_000300: 1.269121e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5513
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5601
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7997
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7647
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3503
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7511
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38163
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

FS
type: SiteQuality
SIO_000300: 3.699e0

DP
type: SiteQuality
SIO_000300: 1.225308e6

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

QD
type: SiteQuality
SIO_000300: 1.546e1

GenotypeQuality
all individuals: 365
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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
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variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7353
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 487
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3348
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.29366106080207e-4
allele num: 7730
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.152874e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

QD
type: SiteQuality
SIO_000300: 1.988e1

GenotypeQuality
all individuals: 5743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5356
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
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: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.902587519025875e-4
allele num: 5256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3311
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7681
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7211
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35867
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 483
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.663e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.811e-1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.145931e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

GenotypeQuality
all individuals: 782
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 662
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variant carriers: 1

GenotypeQuality
all individuals: 3901
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6963
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.953444067392987e-5
allele num: 33594
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.475607936744741e-4
allele num: 6703
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 449
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.023062917256727e-4
allele num: 4943
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3098
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.793e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.112104e6

QD
type: SiteQuality
SIO_000300: 1.402e1

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 3.25e1
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GenotypeQuality
all individuals: 482
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variant carriers: 2

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.649717514124294e-3
allele num: 354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.343e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.91e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.881e0

FS
type: SiteQuality
SIO_000300: 6.791e0

DP
type: SiteQuality
SIO_000300: 3.8207e4

QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 89
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 482
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.073e1

DP
type: SiteQuality
SIO_000300: 3.8062e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.386e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3
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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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 81
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.189060642092747e-3
allele num: 841
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 353
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.377e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.217e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.19e-2

DP
type: SiteQuality
SIO_000300: 3.8085e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 841
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.8328611898017e-3
allele num: 353
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 81
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.26e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

FS
type: SiteQuality
SIO_000300: 2.875e0

MQRankSum
type: SiteQuality
SIO_000300: -9.05e-1

DP
type: SiteQuality
SIO_000300: 3.8151e4

GenotypeQuality
all individuals: 402
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 85
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 81
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.186239620403322e-3
allele num: 843
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.055e0

FS
type: SiteQuality
SIO_000300: 2.621e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 3.8274e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

GenotypeQuality
all individuals: 2126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
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GenotypeQuality
all individuals: 3323
bin: 2.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8201
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5745
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3797
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.629710468877377e-5
allele num: 38027
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.055e1

FS
type: SiteQuality
SIO_000300: 8.054e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -1.895e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.346021e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.105e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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: 4.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5766
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.283697047496791e-4
allele num: 7790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38062
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.59e-1

MQ
type: SiteQuality
SIO_000300: 6.036e1

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 1.909e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

DP
type: SiteQuality
SIO_000300: 1.36218e6

QD
type: SiteQuality
SIO_000300: 1.647e1

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: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5768
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38143
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

FS
type: SiteQuality
SIO_000300: 2.102e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.414e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 1.367314e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3852
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.582444542003461e-5
allele num: 38723
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

DP
type: SiteQuality
SIO_000300: 1.422345e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
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bin: 3.25e1
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
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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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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8645
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.697216564833673e-4
allele num: 5892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3864
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.434048e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

MQ
type: SiteQuality
SIO_000300: 4.475e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 2.92e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 822
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.091649694501019e-5
allele num: 39280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8349
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.424e0

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.47e0

DP
type: SiteQuality
SIO_000300: 1.453642e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.259e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8507
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.946209966613083e-5
allele num: 40435
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3999
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.506398e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.12549240292628e-4
allele num: 8885
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.874006921089828e-5
allele num: 41034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4060
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6149
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 561
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.51e-2

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

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.533e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4119
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8973
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41627
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.60926939169617e-4
allele num: 6214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8668
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.747e1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 2.648e1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6892
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9111
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.340221384943016e-5
allele num: 42731
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4213
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 577
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.144e0

DP
type: SiteQuality
SIO_000300: 1.581273e6

MQ
type: SiteQuality
SIO_000300: 5.843e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

QD
type: SiteQuality
SIO_000300: 1.01e1

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4269
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8321
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6365
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8921
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.088257699423223e-4
allele num: 9189
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.233e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.600452e6

QD
type: SiteQuality
SIO_000300: 3.3e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6425
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.112594570538496e-4
allele num: 8988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44147
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.407e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 9.682e0

DP
type: SiteQuality
SIO_000300: 1.621336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 926
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.221807435059885e-4
allele num: 6429
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.262136361579876e-5
allele num: 44206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8995
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.623357e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.893e0

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 6893
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.255147373880883e-5
allele num: 44343
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6435
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.625813e6

QD
type: SiteQuality
SIO_000300: 3.023e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 770
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1162
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variant carriers: 1

GenotypeQuality
all individuals: 34156
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6447
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.151370679380214e-4
allele num: 8390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4369
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44591
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.833e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 1.257e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.85e-2

DP
type: SiteQuality
SIO_000300: 1.632542e6

GenotypeQuality
all individuals: 776
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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GenotypeQuality
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GenotypeQuality
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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: 1300
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variant carriers: 0

GenotypeQuality
all individuals: 33979
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8393
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.239992832022938e-5
allele num: 44643
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9345
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.408e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.523e0

DP
type: SiteQuality
SIO_000300: 1.635977e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

QD
type: SiteQuality
SIO_000300: 2.409e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4375
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.236335987118705e-5
allele num: 44716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9365
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.074e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.637844e6

QD
type: SiteQuality
SIO_000300: 3.041e1

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
all individuals: 320
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.103752759381898e-4
allele num: 9060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8401
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4385
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6461
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.268e0

MQ
type: SiteQuality
SIO_000300: 5.611e1

DP
type: SiteQuality
SIO_000300: 1.64166e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.468e0

MQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

FS
type: SiteQuality
SIO_000300: 3.566e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.66e-2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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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
all individuals: 828
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4387
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.1033873993159e-4
allele num: 9063
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: 602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6461
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44927
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.417e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

FS
type: SiteQuality
SIO_000300: 2.863e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.121e0

DP
type: SiteQuality
SIO_000300: 1.643198e6

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4788
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6894
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 826
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6467
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8407
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.221235006663705e-5
allele num: 45020
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.256e0

FS
type: SiteQuality
SIO_000300: 7.788e0

DP
type: SiteQuality
SIO_000300: 1.646379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.276e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.75e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.615e0

QD
type: SiteQuality
SIO_000300: 3.231e1

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6893
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 9.25e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6481
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9435
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.209602934352697e-5
allele num: 45257
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4403
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.65381e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.029e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 3.25e1
variant carriers: 4

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

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7076
bin: 9.75e1
variant carriers: 277

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 735
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 541
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4287
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 559
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1319
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 35040
bin: 6.25e1
variant carriers: 5

African
type: Population
allele count: 307
allele frequency: 3.643916913946588e-2
allele num: 8425
num of homozygotes: 6

Latino
type: Population
allele count: 11
allele frequency: 1.209588739828458e-3
allele num: 9094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6491
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.205849913971853e-5
allele num: 45334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9447
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.938e1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

DP
type: SiteQuality
SIO_000300: 1.678269e6

FS
type: SiteQuality
SIO_000300: 5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.753e-1

QD
type: SiteQuality
SIO_000300: 1.656e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

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

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36224
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.098418277680141e-4
allele num: 9104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9491
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.873e1

QD
type: SiteQuality
SIO_000300: 1.29e1

DP
type: SiteQuality
SIO_000300: 1.66909e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-3

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6899
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9108
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.536334306345061e-4
allele num: 6509
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4421
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9497
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45621
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.39e1

DP
type: SiteQuality
SIO_000300: 1.673079e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.317e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

FS
type: SiteQuality
SIO_000300: 1.113e0

GenotypeQuality
all individuals: 36195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9497
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.191972994892703e-5
allele num: 45621
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4421
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.39e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.317e0

DP
type: SiteQuality
SIO_000300: 1.673079e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 1.113e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

GenotypeQuality
all individuals: 6899
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.25886604924328e-4
allele num: 4427
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45663
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.672803e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.016e1

VQSLOD
type: SiteQuality
SIO_000300: -1.979e-1

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

GenotypeQuality
all individuals: 36509
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9119
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.826e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 1.957e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.675756e6

QD
type: SiteQuality
SIO_000300: 4.62e0

MQ
type: SiteQuality
SIO_000300: 5.118e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

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

GenotypeQuality
all individuals: 3987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 547
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9123
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.18595825426945e-4
allele num: 8432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45854
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

DP
type: SiteQuality
SIO_000300: 1.67907e6

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.05e-1

FS
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.5e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6900
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.04887770086008e-4
allele num: 9534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9123
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45854
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

FS
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-1

DP
type: SiteQuality
SIO_000300: 1.67907e6

QD
type: SiteQuality
SIO_000300: 1.5e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9123
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.181358113561504e-5
allele num: 45843
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.763e0

DP
type: SiteQuality
SIO_000300: 1.678877e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.801e0

QD
type: SiteQuality
SIO_000300: 2.116e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -1.97e0

GenotypeQuality
all individuals: 4410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 517
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 547
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36474
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9123
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.181358113561504e-5
allele num: 45843
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.678877e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.801e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 2.116e1

VQSLOD
type: SiteQuality
SIO_000300: -1.97e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 2.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.22e-2

GenotypeQuality
all individuals: 1159
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4407
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36834
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3955
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variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
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variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.179313951967921e-5
allele num: 45886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6513
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4433
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8433
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.499e0

DP
type: SiteQuality
SIO_000300: 1.680815e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 1.0001e1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.232e1

GenotypeQuality
all individuals: 524
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
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variant carriers: 0

GenotypeQuality
all individuals: 412
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variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6899
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9129
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45931
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9555
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4433
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.186661920018987e-4
allele num: 8427
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6505
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 4.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.959e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

FS
type: SiteQuality
SIO_000300: 5.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.465e0

DP
type: SiteQuality
SIO_000300: 1.679568e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 551
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 338
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
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variant carriers: 0

GenotypeQuality
all individuals: 36648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4342
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variant carriers: 0

GenotypeQuality
all individuals: 594
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variant carriers: 1

GenotypeQuality
all individuals: 499
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variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.186802753382388e-4
allele num: 8426
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.096010521701008e-4
allele num: 9124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.178981544026322e-5
allele num: 45893
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.701e0

QD
type: SiteQuality
SIO_000300: 3.058e1

VQSLOD
type: SiteQuality
SIO_000300: -2.05e0

FS
type: SiteQuality
SIO_000300: 1.718e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.31e-2

DP
type: SiteQuality
SIO_000300: 1.678403e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35244
bin: 6.25e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 614
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6958
bin: 9.75e1
variant carriers: 79

GenotypeQuality
all individuals: 571
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4848
bin: 2.25e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 815
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 3.564638783269962e-4
allele num: 8416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 3.167420814479638e-3
allele num: 4420
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.198285337436799e-4
allele num: 9098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6489
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 1.74893970530366e-3
allele num: 45742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9521
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.674967e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.727e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.912e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

QD
type: SiteQuality
SIO_000300: 1.736e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6491
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9105
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45769
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.187930624851509e-4
allele num: 8418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
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: 9518
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.460000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.67228e6

QD
type: SiteQuality
SIO_000300: 1.626e1

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34859
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 591
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6898
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 558
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5713
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6457
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.318826244642269e-4
allele num: 45495
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.103996467211305e-4
allele num: 9058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 1.658434e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.93e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.502e1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeQuality
all individuals: 1141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1273
bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8375
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6421
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4381
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.109877913429523e-4
allele num: 9010
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.685e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.640768e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.901e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 5.312e0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31091
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.498324374170621e-5
allele num: 44461
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4341
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9289
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8919
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6355
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.432e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.782e0

DP
type: SiteQuality
SIO_000300: 1.602928e6

FS
type: SiteQuality
SIO_000300: 6.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.67e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: -1.072e0

GenotypeQuality
all individuals: 1594
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 330
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variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6355
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4341
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8919
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9289
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.249162187085311e-5
allele num: 44461
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.432e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 6.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.782e0

VQSLOD
type: SiteQuality
SIO_000300: -1.072e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 1.602928e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1582
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 1909
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GenotypeQuality
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variant carriers: 41

GenotypeQuality
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GenotypeQuality
all individuals: 201
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 22
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 4000
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6277
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43899
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8865
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9199
num of homozygotes: 0

African
type: Population
allele count: 52
allele frequency: 6.294637453092846e-3
allele num: 8261
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.563164e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.815e1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.458e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 4454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6879
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variant carriers: 3

GenotypeQuality
all individuals: 11758
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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
all individuals: 1023
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5735
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variant carriers: 0

GenotypeQuality
all individuals: 11766
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4141
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8071
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.490807540144287e-4
allele num: 8594
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.173e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 1.39721e6

QD
type: SiteQuality
SIO_000300: 1.71e1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeQuality
all individuals: 1520
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6877
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 530
bin: 8.75e1
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GenotypeQuality
all individuals: 1243
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variant carriers: 0

GenotypeQuality
all individuals: 1100
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variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 2.75e1
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GenotypeQuality
all individuals: 1056
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variant carriers: 0

GenotypeQuality
all individuals: 279
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variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5963
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.148237455505799e-4
allele num: 8709
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4109
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8027
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8533
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41173
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.536e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 3.438e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.384188e6

QD
type: SiteQuality
SIO_000300: 2.366e1

GenotypeQuality
all individuals: 1405
bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.445466105839773e-5
allele num: 40892
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5931
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8005
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 569
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.893e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 6.413e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.375528e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8645
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.454469589121791e-5
allele num: 40742
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.81e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.331e0

FS
type: SiteQuality
SIO_000300: 6.809e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

DP
type: SiteQuality
SIO_000300: 1.372941e6

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1514
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GenotypeQuality
all individuals: 1959
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1342
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variant carriers: 0

GenotypeQuality
all individuals: 4193
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9041
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46693
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.539882968894364e-4
allele num: 6494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.648e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.621023e6

FS
type: SiteQuality
SIO_000300: 3.118e0

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 5.844e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.343e0

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4403
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6497
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.280455440458865e-5
allele num: 46724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9042
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.6e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.503e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 9.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e-1

DP
type: SiteQuality
SIO_000300: 1.645302e6

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.069633115841266e-4
allele num: 46745
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4407
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.248e1

VQSLOD
type: SiteQuality
SIO_000300: -6.284e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 1.660161e6

MQRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 5378
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variant carriers: 1

GenotypeQuality
all individuals: 1345
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.398362019323054e-5
allele num: 46887
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.37925291458482e-4
allele num: 8406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 3.311989401633915e-4
allele num: 9058
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.833e0

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.45e-2

DP
type: SiteQuality
SIO_000300: 1.698917e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

FS
type: SiteQuality
SIO_000300: 8.996e0

QD
type: SiteQuality
SIO_000300: 1.557e1

GenotypeQuality
all individuals: 406
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5467
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variant carriers: 0

GenotypeQuality
all individuals: 1382
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variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1895
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46947
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4417
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.533507130808158e-4
allele num: 6521
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.068e0

QD
type: SiteQuality
SIO_000300: 1.536e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.332e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

DP
type: SiteQuality
SIO_000300: 1.707677e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.97e-1

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 217
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 161
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 42424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47137
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8431
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.202643171806167e-4
allele num: 9080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9823
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.164e1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

FS
type: SiteQuality
SIO_000300: 1.674e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.078e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.730242e6

GenotypeQuality
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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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GenotypeQuality
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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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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47137
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.054056805456582e-4
allele num: 9823
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8431
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.078e0

DP
type: SiteQuality
SIO_000300: 1.730242e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 1.674e0

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.118688955274476e-5
allele num: 47199
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9087
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4433
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.024e1

QD
type: SiteQuality
SIO_000300: 1.27e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 1.73313e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

FS
type: SiteQuality
SIO_000300: 2.762e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4435
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47214
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.301782962799912e-4
allele num: 9086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8441
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6553
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9841
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.122e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

DP
type: SiteQuality
SIO_000300: 1.737038e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.704e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.445e1

FS
type: SiteQuality
SIO_000300: 6.888e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 92
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4182
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GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6561
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8449
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.113807389870635e-5
allele num: 47308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4445
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9881
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9101
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.293e1

FS
type: SiteQuality
SIO_000300: 1.321e0

DP
type: SiteQuality
SIO_000300: 1.743242e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

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

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44374
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9117
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.181055863942365e-4
allele num: 8467
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6579
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: 0
allele frequency: 0.0e0
allele num: 47448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9947
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.755852e6

FS
type: SiteQuality
SIO_000300: 1.002e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: -1.06e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.795e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.039999999999999e0

QD
type: SiteQuality
SIO_000300: 1.476e1

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5740
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1455
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
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: 0
allele frequency: 0.0e0
allele num: 47462
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.096250822188117e-4
allele num: 9122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6581
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.431e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.472e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.204e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 1.756262e6

QD
type: SiteQuality
SIO_000300: 2.623e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.180916391119509e-4
allele num: 8468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4457
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9119
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47465
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6581
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9955
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.381e1

FS
type: SiteQuality
SIO_000300: 6.358e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.257e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.399e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.04e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.919e0

DP
type: SiteQuality
SIO_000300: 1.757138e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

GenotypeQuality
all individuals: 4184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 847
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5769
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.096250822188117e-4
allele num: 9122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8471
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4457
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0