10-82111787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111787
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111787
    reference: chr 10
allele count: 25
allele frequency: 2.063932369064131e-4
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-406G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7216G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-29C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-29C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-29C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-29C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-29C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4266G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

10-82111787-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111787
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111787
    reference: chr 10
allele count: 4
allele frequency: 3.302291790502609e-5
allele num: 121128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4266G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7216G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-29C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-406G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-29C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-29C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-29C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-29C>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-82111788-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111788
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111788
    reference: chr 10
allele count: 15
allele frequency: 1.238400317030481e-4
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7217A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-30T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-30T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-30T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4265A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-405A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-30T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-30T>G
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7538
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

10-82111790-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111790
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111790
    reference: chr 10
allele count: 2
allele frequency: 1.651364026686043e-5
allele num: 121112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-403T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-32A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-32A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-32A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4263T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-32A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7219T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-32A>G
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3467
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

10-82111796-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111796
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111796
    reference: chr 10
allele count: 13
allele frequency: 1.07393638992152e-4
allele num: 121050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-397G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7225G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-38C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4257G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-38C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-38C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-38C>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-38C>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2656
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

10-82111797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111797
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111797
    reference: chr 10
allele count: 10
allele frequency: 8.265965712774223e-5
allele num: 120978
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-39G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-39G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-39G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-39G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7226C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-396C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4256C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-39G>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35992
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5751
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-82111798-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111798
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111798
    reference: chr 10
allele count: 10
allele frequency: 8.264462809917356e-5
allele num: 121000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-40C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-40C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4255G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-395G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-40C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-40C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7227G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-40C>T
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2747
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

10-82111800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111800
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111800
    reference: chr 10
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-42C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-42C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4253G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-42C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7229G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-393G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-42C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-42C>T
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

10-82111805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82111805
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82111805
    reference: chr 10
allele count: 6
allele frequency: 4.966476285075739e-5
allele num: 120810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.148-47G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-4248C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.148-47G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.148-47G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.148-47G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.148-47G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7234C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-388C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

10-82112167-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112167
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112167
    reference: chr 10
allele count: 1
allele frequency: 9.379103357719001e-6
allele num: 106620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+44G>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+44G>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+44G>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7596C>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-26C>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3886C>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+44G>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+44G>C
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13829
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6043
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

10-82112168-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112168
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112168
    reference: chr 10
allele count: 1
allele frequency: 9.353661958656814e-6
allele num: 106910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+43T>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+43T>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+43T>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7597A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+43T>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+43T>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-25A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3885A>G
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16562
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5758
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-82112169-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112169
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112170
    reference: chr 10
allele count: 6
allele frequency: 5.861664712778429e-5
allele num: 102360
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+41dupA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7606dupT
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+41dupA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3876dupT
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-16dupT
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+41dupA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+41dupA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+41dupA
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 1.25e1
  variant carriers: 3
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

10-82112169-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112169
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112168
    reference: chr 10
allele count: 12
allele frequency: 1.172332942555686e-4
allele num: 102360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-16delT
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+41delA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+41delA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7606delT
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+41delA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+41delA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+41delA
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3876delT
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5309
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: GT
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

10-82112170-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112170
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112170
    reference: chr 10
allele count: 1
allele frequency: 9.638925838104602e-6
allele num: 103746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-23T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3883T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+41A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+41A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+41A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+41A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7599T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+41A>C
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 6.75e1
  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: T
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

10-82112171-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112171
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112171
    reference: chr 10
allele count: 1
allele frequency: 9.356637598712527e-6
allele num: 106876
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+40A>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+40A>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7600T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+40A>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3882T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+40A>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-22T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+40A>T
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

10-82112171-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112171
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112171
    reference: chr 10
allele count: 2
allele frequency: 1.871327519742505e-5
allele num: 106876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+40A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7600T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+40A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+40A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-22T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+40A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+40A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3882T>G
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

10-82112177-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112177
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112177
    reference: chr 10
allele count: 6
allele frequency: 5.56379821958457e-5
allele num: 107840
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+34A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+34A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7606T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+34A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+34A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-16T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3876T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+34A>G
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11577
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21242
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

10-82112188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112188
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112188
    reference: chr 10
allele count: 1
allele frequency: 9.12258935576274e-6
allele num: 109618
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7617C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+23G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-527-5C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3865C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+23G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+23G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+23G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+23G>A
  variant of: http://identifiers.org/hgnc/23460
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5555
  bin: 2.25e1
  variant carriers: 0
hgvs: c.-527-5C>T
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

10-82112201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112201
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112201
    reference: chr 10
allele count: 1
allele frequency: 8.802506953980493e-6
allele num: 113604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3852T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7630T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+10A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+10A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-519T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+10A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+10A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+10A>G
  variant of: http://identifiers.org/hgnc/23460
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11514
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

10-82112206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112206
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112206
    reference: chr 10
allele count: 1
allele frequency: 8.720220447172904e-6
allele num: 114676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+5G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3847C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-514C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+5G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+5G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7635C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+5G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+5G>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
hgvs: c.147+5G>A
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: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-82112210-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112210
    reference: chr 10
allele count: 1
allele frequency: 8.660408078428655e-6
allele num: 115468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+1G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+1G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+1G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7639C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3843C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+1G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-510C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+1G>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
hgvs: c.147+1G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/10-82112210-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112210
    reference: chr 10
allele count: 1
allele frequency: 8.660408078428655e-6
allele num: 115468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-510C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.147+1G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.147+1G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3843C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.147+1G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.147+1G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7639C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.147+1G>T
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12232
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
hgvs: c.147+1G>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-82112212-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112212
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112212
    reference: chr 10
allele count: 3
allele frequency: 2.589421350642176e-5
allele num: 115856
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7641A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.146T>G
  hgvsp: ENSP00000361276.1:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.146T>G
  hgvsp: ENSP00000388160.1:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-508A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.146T>G
  hgvsp: ENSP00000414798.1:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.146T>G
  hgvsp: ENSP00000402890.2:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3841A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.146T>G
  hgvsp: ENSP00000361278.3:p.Leu49Arg
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43053
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu49Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

10-82112214-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112214
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112214
    reference: chr 10
allele count: 1
allele frequency: 8.61489687968435e-6
allele num: 116078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.144A>T
  hgvsp: ENSP00000414798.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.144A>T
  hgvsp: ENSP00000361278.3:p.Gln48His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3839T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7643T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-506T>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.144A>T
  hgvsp: ENSP00000361276.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.144A>T
  hgvsp: ENSP00000388160.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.144A>T
  hgvsp: ENSP00000402890.2:p.Gln48His
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln48His
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

10-82112216-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112216
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112216
    reference: chr 10
allele count: 1
allele frequency: 8.59697386519945e-6
allele num: 116320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.142C>A
  hgvsp: ENSP00000388160.1:p.Gln48Lys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3837G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7645G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-504G>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.142C>A
  hgvsp: ENSP00000414798.1:p.Gln48Lys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.142C>A
  hgvsp: ENSP00000361276.1:p.Gln48Lys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.142C>A
  hgvsp: ENSP00000402890.2:p.Gln48Lys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.142C>A
  hgvsp: ENSP00000361278.3:p.Gln48Lys
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln48Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

10-82112229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112229
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112229
    reference: chr 10
allele count: 1
allele frequency: 8.489396743467409e-6
allele num: 117794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3824A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.129T>C
  hgvsp: ENST00000453477.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7658A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.129T>C
  hgvsp: ENST00000372204.3:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.129T>C
  hgvsp: ENST00000454362.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-491A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.129T>C
  hgvsp: ENST00000421924.2:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.129T>C
  hgvsp: ENST00000372202.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43785
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn43Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

10-82112244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112244
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112244
    reference: chr 10
allele count: 1
allele frequency: 8.4199181583955e-6
allele num: 118766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.114C>T
  hgvsp: ENST00000453477.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.114C>T
  hgvsp: ENST00000372202.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7673G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3809G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.114C>T
  hgvsp: ENST00000454362.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.114C>T
  hgvsp: ENST00000421924.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.114C>T
  hgvsp: ENST00000372204.3:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-476G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr38Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-82112260-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112260
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112260
    reference: chr 10
allele count: 2
allele frequency: 1.673920321392702e-5
allele num: 119480
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.98T>C
  hgvsp: ENSP00000402890.2:p.Leu33Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.98T>C
  hgvsp: ENSP00000388160.1:p.Leu33Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3793A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.98T>C
  hgvsp: ENSP00000361278.3:p.Leu33Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.98T>C
  hgvsp: ENSP00000361276.1:p.Leu33Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-460A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7689A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.98T>C
  hgvsp: ENSP00000414798.1:p.Leu33Ser
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu33Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

10-82112260-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112260
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112260
    reference: chr 10
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.98T>A
  hgvsp: ENSP00000414798.1:p.Leu33Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.98T>A
  hgvsp: ENSP00000388160.1:p.Leu33Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.98T>A
  hgvsp: ENSP00000402890.2:p.Leu33Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.98T>A
  hgvsp: ENSP00000361278.3:p.Leu33Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3793A>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-460A>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7689A>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.98T>A
  hgvsp: ENSP00000361276.1:p.Leu33Ter
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu33Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

10-82112269-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112269
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112269
    reference: chr 10
allele count: 1
allele frequency: 8.344180768332166e-6
allele num: 119844
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.89T>C
  hgvsp: ENSP00000361278.3:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3784A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.89T>C
  hgvsp: ENSP00000388160.1:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.89T>C
  hgvsp: ENSP00000361276.1:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-451A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.89T>C
  hgvsp: ENSP00000414798.1:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.89T>C
  hgvsp: ENSP00000402890.2:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7698A>G
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile30Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-82112271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112271
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112271
    reference: chr 10
allele count: 9
allele frequency: 7.505629221916437e-5
allele num: 119910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.87G>A
  hgvsp: ENST00000421924.2:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.87G>A
  hgvsp: ENST00000454362.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.87G>A
  hgvsp: ENST00000372202.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7700C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.87G>A
  hgvsp: ENST00000453477.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.87G>A
  hgvsp: ENST00000372204.3:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-449C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3782C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35606
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15458
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2291
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro29Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

10-82112277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112277
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112277
    reference: chr 10
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7706C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.81G>A
  hgvsp: ENST00000454362.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.81G>A
  hgvsp: ENST00000372202.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.81G>A
  hgvsp: ENST00000421924.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3776C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.81G>A
  hgvsp: ENST00000453477.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.81G>A
  hgvsp: ENST00000372204.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-443C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val27Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

10-82112279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112279
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112279
    reference: chr 10
allele count: 22
allele frequency: 1.828335881922745e-4
allele num: 120328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.79G>A
  hgvsp: ENSP00000361276.1:p.Val27Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.79G>A
  hgvsp: ENSP00000402890.2:p.Val27Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.79G>A
  hgvsp: ENSP00000361278.3:p.Val27Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.79G>A
  hgvsp: ENSP00000414798.1:p.Val27Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-441C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.79G>A
  hgvsp: ENSP00000388160.1:p.Val27Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3774C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7708C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35701
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15851
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5098
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val27Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

10-82112280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112280
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112280
    reference: chr 10
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-440T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7709T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.78A>G
  hgvsp: ENST00000372202.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.78A>G
  hgvsp: ENST00000454362.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.78A>G
  hgvsp: ENST00000453477.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3773T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.78A>G
  hgvsp: ENST00000372204.3:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.78A>G
  hgvsp: ENST00000421924.2:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro26Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

10-82112281-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112281
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112281
    reference: chr 10
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.77C>G
  hgvsp: ENSP00000414798.1:p.Pro26Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.77C>G
  hgvsp: ENSP00000402890.2:p.Pro26Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3772G>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.77C>G
  hgvsp: ENSP00000361278.3:p.Pro26Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.77C>G
  hgvsp: ENSP00000361276.1:p.Pro26Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.77C>G
  hgvsp: ENSP00000388160.1:p.Pro26Arg
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-439G>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7710G>C
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5113
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro26Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-82112284-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112284
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112284
    reference: chr 10
allele count: 2
allele frequency: 1.660881263598465e-5
allele num: 120418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.74G>T
  hgvsp: ENSP00000402890.2:p.Arg25Leu
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.74G>T
  hgvsp: ENSP00000414798.1:p.Arg25Leu
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-436C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.74G>T
  hgvsp: ENSP00000361276.1:p.Arg25Leu
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.74G>T
  hgvsp: ENSP00000388160.1:p.Arg25Leu
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7713C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.74G>T
  hgvsp: ENSP00000361278.3:p.Arg25Leu
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3769C>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg25Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP

10-82112284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112284
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112284
    reference: chr 10
allele count: 6
allele frequency: 4.982643790795396e-5
allele num: 120418
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7713C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-436C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.74G>A
  hgvsp: ENSP00000361278.3:p.Arg25His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.74G>A
  hgvsp: ENSP00000361276.1:p.Arg25His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.74G>A
  hgvsp: ENSP00000388160.1:p.Arg25His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3769C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.74G>A
  hgvsp: ENSP00000414798.1:p.Arg25His
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.74G>A
  hgvsp: ENSP00000402890.2:p.Arg25His
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5112
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg25His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

10-82112285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112285
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112285
    reference: chr 10
allele count: 3
allele frequency: 2.490205192907896e-5
allele num: 120472
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.73C>T
  hgvsp: ENSP00000361278.3:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.73C>T
  hgvsp: ENSP00000361276.1:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.73C>T
  hgvsp: ENSP00000402890.2:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.73C>T
  hgvsp: ENSP00000388160.1:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3768G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-435G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7714G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.73C>T
  hgvsp: ENSP00000414798.1:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg25Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

10-82112295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112295
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112295
    reference: chr 10
allele count: 2
allele frequency: 1.656973372437905e-5
allele num: 120702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.63G>A
  hgvsp: ENST00000372202.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.63G>A
  hgvsp: ENST00000421924.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.63G>A
  hgvsp: ENST00000454362.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.63G>A
  hgvsp: ENST00000453477.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-425C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.63G>A
  hgvsp: ENST00000372204.3:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3758C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7724C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35653
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val21Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

10-82112296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112296
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112296
    reference: chr 10
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.62T>C
  hgvsp: ENSP00000402890.2:p.Val21Ala
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-424A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.62T>C
  hgvsp: ENSP00000361276.1:p.Val21Ala
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.62T>C
  hgvsp: ENSP00000388160.1:p.Val21Ala
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.62T>C
  hgvsp: ENSP00000361278.3:p.Val21Ala
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.62T>C
  hgvsp: ENSP00000414798.1:p.Val21Ala
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3757A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7725A>G
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val21Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

10-82112297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112297
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112297
    reference: chr 10
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7726C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3756C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.61G>A
  hgvsp: ENSP00000402890.2:p.Val21Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.61G>A
  hgvsp: ENSP00000361276.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.61G>A
  hgvsp: ENSP00000388160.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.61G>A
  hgvsp: ENSP00000361278.3:p.Val21Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.61G>A
  hgvsp: ENSP00000414798.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-423C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val21Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

10-82112309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112309
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112309
    reference: chr 10
allele count: 1
allele frequency: 8.273625337150233e-6
allele num: 120866
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.49G>A
  hgvsp: ENSP00000361278.3:p.Gly17Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-411C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.49G>A
  hgvsp: ENSP00000388160.1:p.Gly17Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.49G>A
  hgvsp: ENSP00000361276.1:p.Gly17Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7738C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3744C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.49G>A
  hgvsp: ENSP00000414798.1:p.Gly17Ser
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.49G>A
  hgvsp: ENSP00000402890.2:p.Gly17Ser
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35610
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly17Ser
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-82112314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112314
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112314
    reference: chr 10
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.44C>T
  hgvsp: ENSP00000361276.1:p.Thr15Ile
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3739G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-406G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.44C>T
  hgvsp: ENSP00000361278.3:p.Thr15Ile
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.44C>T
  hgvsp: ENSP00000402890.2:p.Thr15Ile
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7743G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.44C>T
  hgvsp: ENSP00000414798.1:p.Thr15Ile
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.44C>T
  hgvsp: ENSP00000388160.1:p.Thr15Ile
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr15Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

10-82112329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112329
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112329
    reference: chr 10
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-391A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.29T>C
  hgvsp: ENSP00000388160.1:p.Leu10Pro
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.29T>C
  hgvsp: ENSP00000414798.1:p.Leu10Pro
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.29T>C
  hgvsp: ENSP00000361276.1:p.Leu10Pro
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3724A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7758A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.29T>C
  hgvsp: ENSP00000402890.2:p.Leu10Pro
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.29T>C
  hgvsp: ENSP00000361278.3:p.Leu10Pro
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48002
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu10Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-82112330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112330
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112330
    reference: chr 10
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.28C>T
  hgvsp: ENSP00000388160.1:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.28C>T
  hgvsp: ENSP00000361276.1:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.28C>T
  hgvsp: ENSP00000361278.3:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-390G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.28C>T
  hgvsp: ENSP00000414798.1:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7759G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.28C>T
  hgvsp: ENSP00000402890.2:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3723G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu10Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

10-82112335-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112335
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112335
    reference: chr 10
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.23A>C
  hgvsp: ENSP00000402890.2:p.Lys8Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3718T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.23A>C
  hgvsp: ENSP00000361276.1:p.Lys8Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.23A>C
  hgvsp: ENSP00000361278.3:p.Lys8Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7764T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.23A>C
  hgvsp: ENSP00000414798.1:p.Lys8Thr
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-385T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.23A>C
  hgvsp: ENSP00000388160.1:p.Lys8Thr
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5093
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys8Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

10-82112339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112339
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112339
    reference: chr 10
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.19C>T
  hgvsp: ENSP00000361276.1:p.Gln7Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.19C>T
  hgvsp: ENSP00000361278.3:p.Gln7Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.19C>T
  hgvsp: ENSP00000414798.1:p.Gln7Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.19C>T
  hgvsp: ENSP00000402890.2:p.Gln7Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3714G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.19C>T
  hgvsp: ENSP00000388160.1:p.Gln7Ter
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-381G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7768G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16787
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln7Ter
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

10-82112342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112342
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112342
    reference: chr 10
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.16C>T
  hgvsp: ENSP00000361278.3:p.Leu6Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.16C>T
  hgvsp: ENSP00000402890.2:p.Leu6Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.16C>T
  hgvsp: ENSP00000414798.1:p.Leu6Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-378G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.16C>T
  hgvsp: ENSP00000388160.1:p.Leu6Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3711G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.16C>T
  hgvsp: ENSP00000361276.1:p.Leu6Phe
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7771G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16792
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu6Phe
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

10-82112360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112360
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112360
    reference: chr 10
allele count: 1
allele frequency: 8.406469619018796e-6
allele num: 118956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-360C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7789C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-3G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3693C>T
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4780
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

10-82112365-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112365
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112365
    reference: chr 10
allele count: 1
allele frequency: 8.433125316242199e-6
allele num: 118580
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3688T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-355T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-8A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7794T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-8A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-8A>C
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15727
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42864
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
hgvs: c.-8A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

10-82112378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112378
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112378
    reference: chr 10
allele count: 1
allele frequency: 8.508900309723971e-6
allele num: 117524
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-12C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-12C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-12C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-12C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+5G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7807G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-12C>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3675G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
hgvs: c.-347+5G>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

10-82112379-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112379
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112379
    reference: chr 10
allele count: 1
allele frequency: 8.520064752492119e-6
allele num: 117370
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-13A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-13A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3674T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-13A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+6T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-13A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7808T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-13A>G
  variant of: http://identifiers.org/hgnc/23460
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6260
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 9.25e1
  variant carriers: 0
hgvs: c.-347+6T>C
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

10-82112385-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112385
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112385
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 116746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3668T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-19A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7814T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-19A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+12T>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-19A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-19A>C
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-19A>C
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-82112387-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112387
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112387
    reference: chr 10
allele count: 1
allele frequency: 8.583690987124463e-6
allele num: 116500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-21G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-21G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+14C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-21G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7816C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3666C>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-21G>T
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-21G>T
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-82112391-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112391
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112391
    reference: chr 10
allele count: 1
allele frequency: 8.602150537634409e-6
allele num: 116250
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7820A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-25T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-25T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3662A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+18A>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-25T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-25T>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-25T>G
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-82112395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112395
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112395
    reference: chr 10
allele count: 8
allele frequency: 6.92508786205225e-5
allele num: 115522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-29G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3658C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-29G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7824C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+22C>T
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-29G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-29G>A
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-29G>A
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13837
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9447
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8196
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6943
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-82112402-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82112402
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82112402
    reference: chr 10
allele count: 2
allele frequency: 1.74800727171025e-5
allele num: 114416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-309-3651T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000388160
  ensembl transcript: ENST00000453477
  gene symbol: DYDC1
  hgvsc: ENST00000453477.1:c.-9-36A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-347+29T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361278
  ensembl transcript: ENST00000372204
  gene symbol: DYDC1
  hgvsc: ENST00000372204.3:c.-9-36A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000402890
  ensembl transcript: ENST00000421924
  gene symbol: DYDC1
  hgvsc: ENST00000421924.2:c.-9-36A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000414798
  ensembl transcript: ENST00000454362
  gene symbol: DYDC1
  hgvsc: ENST00000454362.1:c.-9-36A>G
  variant of: http://identifiers.org/hgnc/23460
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.33+7831T>C
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170788
  ensembl protein: ENSP00000361276
  ensembl transcript: ENST00000372202
  gene symbol: DYDC1
  hgvsc: ENST00000372202.1:c.-9-36A>G
  variant of: http://identifiers.org/hgnc/23460
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7664
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7866
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-82122161-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122161
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122161
    reference: chr 10
allele count: 1
allele frequency: 8.461668641056017e-6
allele num: 118180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.-9-30A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-9-30A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-9-30A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.34-30A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.-9-30A>G
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.-9-30A>G
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3039
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19095
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-82122164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122164
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122164
    reference: chr 10
allele count: 1
allele frequency: 8.453657052040712e-6
allele num: 118292
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.34-27G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.-9-27G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-9-27G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-9-27G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.-9-27G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.-9-27G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

10-82122168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122168
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122168
    reference: chr 10
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.34-23G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.-9-23G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.-9-23G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.-9-23G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.-9-23G>A
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.-9-23G>A
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

10-82122206-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122206
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122206
    reference: chr 10
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.7A>T
  hgvsp: ENSP00000401333.1:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.7A>T
  hgvsp: ENSP00000361271.1:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.7A>T
  hgvsp: ENSP00000256039.2:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.7A>T
  hgvsp: ENSP00000410285.2:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.7A>T
  hgvsp: ENSP00000361273.1:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.49A>T
  hgvsp: ENSP00000361272.1:p.Thr17Ser
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3546
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr17Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

10-82122208-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122208
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122207
    reference: chr 10
allele count: 2
allele frequency: 1.651909607506277e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.11delA
  hgvsp: ENSP00000256039.2:p.Asn4ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.11delA
  hgvsp: ENSP00000361273.1:p.Asn4ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.11delA
  hgvsp: ENSP00000401333.1:p.Asn4ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.11delA
  hgvsp: ENSP00000361271.1:p.Asn4ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.11delA
  hgvsp: ENSP00000410285.2:p.Asn4ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.53delA
  hgvsp: ENSP00000361272.1:p.Asn18ThrfsTer3
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9002
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6173
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn18ThrfsTer3
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: TA
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-82122214-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122214
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122214
    reference: chr 10
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.57C>G
  hgvsp: ENSP00000361272.1:p.Tyr19Ter
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.15C>G
  hgvsp: ENSP00000410285.2:p.Tyr5Ter
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.15C>G
  hgvsp: ENSP00000401333.1:p.Tyr5Ter
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.15C>G
  hgvsp: ENSP00000256039.2:p.Tyr5Ter
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.15C>G
  hgvsp: ENSP00000361271.1:p.Tyr5Ter
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.15C>G
  hgvsp: ENSP00000361273.1:p.Tyr5Ter
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr19Ter
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

10-82122221-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122221
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122221
    reference: chr 10
allele count: 4
allele frequency: 3.299894403379092e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.22A>T
  hgvsp: ENSP00000401333.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.22A>T
  hgvsp: ENSP00000256039.2:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.64A>T
  hgvsp: ENSP00000361272.1:p.Arg22Trp
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.22A>T
  hgvsp: ENSP00000410285.2:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.22A>T
  hgvsp: ENSP00000361271.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.22A>T
  hgvsp: ENSP00000361273.1:p.Arg8Trp
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3071
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17023
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg22Trp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

10-82122223-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122223
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122223
    reference: chr 10
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.24G>T
  hgvsp: ENSP00000361273.1:p.Arg8Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.66G>T
  hgvsp: ENSP00000361272.1:p.Arg22Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.24G>T
  hgvsp: ENSP00000401333.1:p.Arg8Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.24G>T
  hgvsp: ENSP00000256039.2:p.Arg8Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.24G>T
  hgvsp: ENSP00000410285.2:p.Arg8Ser
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.24G>T
  hgvsp: ENSP00000361271.1:p.Arg8Ser
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6187
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg22Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-82122241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122241
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122241
    reference: chr 10
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.42G>A
  hgvsp: ENST00000411538.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.42G>A
  hgvsp: ENST00000372197.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.42G>A
  hgvsp: ENST00000256039.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.42G>A
  hgvsp: ENST00000372199.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.42G>A
  hgvsp: ENST00000444807.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.84G>A
  hgvsp: ENST00000372198.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3070
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu28Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

10-82122242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122242
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122242
    reference: chr 10
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.43G>A
  hgvsp: ENSP00000361273.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.43G>A
  hgvsp: ENSP00000256039.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.43G>A
  hgvsp: ENSP00000410285.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.43G>A
  hgvsp: ENSP00000361271.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.85G>A
  hgvsp: ENSP00000361272.1:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.43G>A
  hgvsp: ENSP00000401333.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13192
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala29Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-82122249-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122249
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122249
    reference: chr 10
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.50C>G
  hgvsp: ENSP00000361271.1:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.50C>G
  hgvsp: ENSP00000361273.1:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.50C>G
  hgvsp: ENSP00000410285.2:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.92C>G
  hgvsp: ENSP00000361272.1:p.Ala31Gly
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.50C>G
  hgvsp: ENSP00000401333.1:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.50C>G
  hgvsp: ENSP00000256039.2:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19085
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala31Gly
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-82122255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122255
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122255
    reference: chr 10
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.56C>T
  hgvsp: ENSP00000410285.2:p.Ala19Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.56C>T
  hgvsp: ENSP00000361273.1:p.Ala19Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.56C>T
  hgvsp: ENSP00000361271.1:p.Ala19Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.56C>T
  hgvsp: ENSP00000256039.2:p.Ala19Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.56C>T
  hgvsp: ENSP00000401333.1:p.Ala19Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.98C>T
  hgvsp: ENSP00000361272.1:p.Ala33Val
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala33Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-82122256-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122256
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122256
    reference: chr 10
allele count: 3
allele frequency: 2.472595400972554e-5
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.57A>G
  hgvsp: ENST00000411538.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.57A>G
  hgvsp: ENST00000444807.2:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.99A>G
  hgvsp: ENST00000372198.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.57A>G
  hgvsp: ENST00000256039.2:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.57A>G
  hgvsp: ENST00000372197.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.57A>G
  hgvsp: ENST00000372199.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6183
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala33Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

10-82122264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82122264
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 82122264
    reference: chr 10
allele count: 10
allele frequency: 8.243207596940122e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361271
  ensembl transcript: ENST00000372197
  gene symbol: DYDC2
  hgvsc: ENST00000372197.1:c.65C>T
  hgvsp: ENSP00000361271.1:p.Ala22Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000256039
  ensembl transcript: ENST00000256039
  gene symbol: DYDC2
  hgvsc: ENST00000256039.2:c.65C>T
  hgvsp: ENSP00000256039.2:p.Ala22Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000410285
  ensembl transcript: ENST00000444807
  gene symbol: DYDC2
  hgvsc: ENST00000444807.2:c.65C>T
  hgvsp: ENSP00000410285.2:p.Ala22Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361273
  ensembl transcript: ENST00000372199
  gene symbol: DYDC2
  hgvsc: ENST00000372199.1:c.65C>T
  hgvsp: ENSP00000361273.1:p.Ala22Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000401333
  ensembl transcript: ENST00000411538
  gene symbol: DYDC2
  hgvsc: ENST00000411538.1:c.65C>T
  hgvsp: ENSP00000401333.1:p.Ala22Val
  variant of: http://identifiers.org/hgnc/23468
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133665
  ensembl protein: ENSP00000361272
  ensembl transcript: ENST00000372198
  gene symbol: DYDC2
  hgvsc: ENST00000372198.1:c.107C>T
  hgvsp: ENSP00000361272.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/23468
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12224
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3535
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17087
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala36Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C

GenotypeQuality
all individuals: 1716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36016
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 3047
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.926411096127914e-4
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.452831321683781e-4
allele num: 66612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.383e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 2.90475e6

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36016
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7584
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.852822192255828e-4
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.90475e6

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.383e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

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

GenotypeQuality
all individuals: 7319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36005
bin: 9.75e1
variant carriers: 15

African
type: Population
allele count: 13
allele frequency: 1.252408477842004e-3
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.493e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.90091e6

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 8
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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: 165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36000
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3045
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.220256253813301e-4
allele num: 16390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.679e0

DP
type: SiteQuality
SIO_000300: 2.897595e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.536e1

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

GenotypeQuality
all individuals: 368
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35993
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 406
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variant carriers: 0

GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 1496
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variant carriers: 0

GenotypeQuality
all individuals: 780
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variant carriers: 0

GenotypeQuality
all individuals: 3466
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variant carriers: 0

GenotypeQuality
all individuals: 2771
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variant carriers: 0

GenotypeQuality
all individuals: 394
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variant carriers: 0

GenotypeQuality
all individuals: 6009
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.643201542912247e-4
allele num: 10370
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.35e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.225e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 2.886635e6

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 1489
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variant carriers: 0

GenotypeQuality
all individuals: 828
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variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 3039
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variant carriers: 0

GenotypeQuality
all individuals: 2624
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variant carriers: 0

GenotypeQuality
all individuals: 2755
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variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.122199093914534e-4
allele num: 16334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.884776e6

QD
type: SiteQuality
SIO_000300: 1.426e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 3037
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 3464
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 35978
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variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 855
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.119202056051891e-5
allele num: 16342
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.098102730217492e-4
allele num: 8644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.882787e6

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.827e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
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variant carriers: 0

GenotypeQuality
all individuals: 3036
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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
all individuals: 2735
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variant carriers: 0

GenotypeQuality
all individuals: 2598
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variant carriers: 0

GenotypeQuality
all individuals: 1484
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variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.282e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 3.144e0

DP
type: SiteQuality
SIO_000300: 2.879089e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
all individuals: 852
bin: 3.25e1
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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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 1461
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GenotypeQuality
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GenotypeQuality
all individuals: 759
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GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2462
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.02337052967185e-5
allele num: 66494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

QD
type: SiteQuality
SIO_000300: 1.394e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e0

DP
type: SiteQuality
SIO_000300: 2.872559e6

GenotypeQuality
all individuals: 3046
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1182
bin: 7.25e1
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GenotypeQuality
all individuals: 731
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variant carriers: 0

GenotypeQuality
all individuals: 144
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GenotypeQuality
all individuals: 5454
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variant carriers: 0

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 3782
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variant carriers: 0

GenotypeQuality
all individuals: 5844
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variant carriers: 0

GenotypeQuality
all individuals: 4212
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.493070058857034e-5
allele num: 10534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 1.564e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

QD
type: SiteQuality
SIO_000300: 1.014e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.200526e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 612
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3015
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.018744906275469e-4
allele num: 9816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.205867e6

VQSLOD
type: SiteQuality
SIO_000300: -1.523e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.838e0

QD
type: SiteQuality
SIO_000300: 1.188e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.148e0

GenotypeQuality
all individuals: 6056
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 992
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.132753707898006e-5
allele num: 54748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.044059302568386e-4
allele num: 9578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 4.54e0

DP
type: SiteQuality
SIO_000300: 1.224096e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

FS
type: SiteQuality
SIO_000300: 1.119e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

GenotypeQuality
all individuals: 6056
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5496
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 879
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 7

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.132753707898006e-5
allele num: 54748
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.200594353640416e-4
allele num: 13460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 1.119e0

QD
type: SiteQuality
SIO_000300: 4.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

DP
type: SiteQuality
SIO_000300: 1.224096e6

GenotypeQuality
all individuals: 1016
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5427
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
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variant carriers: 0

GenotypeQuality
all individuals: 2619
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variant carriers: 0

GenotypeQuality
all individuals: 328
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variant carriers: 0

GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19707
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variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1397
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13662
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55480
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.225994e6

VQSLOD
type: SiteQuality
SIO_000300: -2.748e0

FS
type: SiteQuality
SIO_000300: 6.107e0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

GenotypeQuality
all individuals: 569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
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variant carriers: 0

GenotypeQuality
all individuals: 766
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variant carriers: 0

GenotypeQuality
all individuals: 2284
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variant carriers: 1

GenotypeQuality
all individuals: 3259
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
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variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22148
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variant carriers: 0

GenotypeQuality
all individuals: 1215
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variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.017543859649122e-5
allele num: 14250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.229439e6

QD
type: SiteQuality
SIO_000300: 1.894e1

VQSLOD
type: SiteQuality
SIO_000300: -8.250999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e0

FS
type: SiteQuality
SIO_000300: 1.351e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5113
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.495281370150297e-5
allele num: 57220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 1.351e0

VQSLOD
type: SiteQuality
SIO_000300: -8.250999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

QD
type: SiteQuality
SIO_000300: 1.894e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.229439e6

GenotypeQuality
all individuals: 1837
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6060
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2680
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variant carriers: 0

GenotypeQuality
all individuals: 3952
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 350
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variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.038709230662697e-4
allele num: 57764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.254196e6

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
all individuals: 414
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
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GenotypeQuality
all individuals: 199
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GenotypeQuality
all individuals: 717
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GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2228
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 34581
bin: 6.25e1
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GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699639676388606e-5
allele num: 58836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14708
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.406e0

VQSLOD
type: SiteQuality
SIO_000300: -1.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 7.46e0

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

MQ
type: SiteQuality
SIO_000300: 5.728e1

DP
type: SiteQuality
SIO_000300: 1.337756e6

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 340
bin: 4.75e1
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GenotypeQuality
all individuals: 1291
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variant carriers: 0

GenotypeQuality
all individuals: 460
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variant carriers: 0

GenotypeQuality
all individuals: 4595
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variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628664495114006e-5
allele num: 61400
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.41e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 1.413922e6

GenotypeQuality
all individuals: 1218
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4646
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610409688224684e-5
allele num: 62096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11202
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.431737e6

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.914e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.597035901367063e-5
allele num: 62616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.77e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.444479e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.003e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

GenotypeQuality
all individuals: 2974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.597035901367063e-5
allele num: 62616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15536
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.101e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.444479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

FS
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.003e0

GenotypeQuality
all individuals: 2817
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.75e1
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
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.77190303493033e-5
allele num: 62868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.461e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 4.679e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.449892e6

QD
type: SiteQuality
SIO_000300: 1.098e1

VQSLOD
type: SiteQuality
SIO_000300: 9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 43001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
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variant carriers: 0

GenotypeQuality
all individuals: 2728
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 2284
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variant carriers: 1

GenotypeQuality
all individuals: 550
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586646780693682e-5
allele num: 63026
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.453198e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

FS
type: SiteQuality
SIO_000300: 1.761e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.696e1

QD
type: SiteQuality
SIO_000300: 1.193e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.566e0

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42985
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 2626
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variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 406
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.107e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.283e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.456643e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

GenotypeQuality
all individuals: 1307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.264094211976948e-5
allele num: 15964
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.22e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

DP
type: SiteQuality
SIO_000300: 1.477637e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.169e0

FS
type: SiteQuality
SIO_000300: 7.663e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.604e0

QD
type: SiteQuality
SIO_000300: 1.052e1

GenotypeQuality
all individuals: 2286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540594669542443e-5
allele num: 64910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: -9.877e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

DP
type: SiteQuality
SIO_000300: 1.494015e6

FS
type: SiteQuality
SIO_000300: 3.067e0

QD
type: SiteQuality
SIO_000300: 1.011e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeQuality
all individuals: 5033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 784
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variant carriers: 0

GenotypeQuality
all individuals: 45412
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variant carriers: 0

GenotypeQuality
all individuals: 469
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 563
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.237164419151305e-4
allele num: 16166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65458
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.877e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

DP
type: SiteQuality
SIO_000300: 1.509019e6

FS
type: SiteQuality
SIO_000300: 1.214e0

QD
type: SiteQuality
SIO_000300: 1.307e1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.589e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

GenotypeQuality
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bin: 1.75e1
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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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65458
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.214e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.509019e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.589e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65726
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.516356e6

QD
type: SiteQuality
SIO_000300: 2.301e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.67e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.368197020370934e-4
allele num: 65780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.187e1

DP
type: SiteQuality
SIO_000300: 1.519343e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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
all individuals: 257
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514417252241338e-5
allele num: 66032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.524693e6

QD
type: SiteQuality
SIO_000300: 1.244e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.949e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

GenotypeQuality
all individuals: 677
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 22

GenotypeQuality
all individuals: 275
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.664699294772844e-4
allele num: 66078
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.83289817232376e-4
allele num: 11490
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.866e0

DP
type: SiteQuality
SIO_000300: 1.525986e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

FS
type: SiteQuality
SIO_000300: 1.738e0

VQSLOD
type: SiteQuality
SIO_000300: 4.48e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66120
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.295e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 2.647e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.38e-1

DP
type: SiteQuality
SIO_000300: 1.526612e6

QD
type: SiteQuality
SIO_000300: 1.397e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66114
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.22e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

DP
type: SiteQuality
SIO_000300: 1.527267e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023797284630038e-5
allele num: 66142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 2.445e0

DP
type: SiteQuality
SIO_000300: 1.52965e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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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: 212
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 228
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.047594569260077e-5
allele num: 66142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73973556019485e-4
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

FS
type: SiteQuality
SIO_000300: 2.445e0

DP
type: SiteQuality
SIO_000300: 1.52965e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 246
bin: 5.25e1
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: 3.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 2281
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.352e1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

DP
type: SiteQuality
SIO_000300: 1.530276e6

MQ
type: SiteQuality
SIO_000300: 5.909e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016045361322234e-5
allele num: 66312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.634e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.534422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

MQ
type: SiteQuality
SIO_000300: 5.884e1

FS
type: SiteQuality
SIO_000300: 2.109e0

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.59e0

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

GenotypeQuality
all individuals: 5153
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
all individuals: 47760
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.09979260705136e-5
allele num: 16394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.144e0

DP
type: SiteQuality
SIO_000300: 1.534274e6

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.208e0

QD
type: SiteQuality
SIO_000300: 5.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.83e-1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
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variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 9.75e1
variant carriers: 1

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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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507340749449821e-5
allele num: 66342
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.681e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.147e0

QD
type: SiteQuality
SIO_000300: 1.163e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

DP
type: SiteQuality
SIO_000300: 1.534452e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2278
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.536984e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.915e1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 81
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

FS
type: SiteQuality
SIO_000300: 2.527e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

DP
type: SiteQuality
SIO_000300: 1.537323e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.219e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

FS
type: SiteQuality
SIO_000300: 4.299e0

DP
type: SiteQuality
SIO_000300: 1.535623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.504e0

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.901e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 2.711e1

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1299
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.92e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.378e0

MQRankSum
type: SiteQuality
SIO_000300: -1.258e0

MQ
type: SiteQuality
SIO_000300: 4.465e1

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.533667e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.214e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.81e-1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509069507741527e-5
allele num: 66266
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 5.6587e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: -1.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.883e0

DP
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QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 4.098e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 1.529022e6

FS
type: SiteQuality
SIO_000300: 5.3538e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 6.72e0

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

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.524111443028714e-5
allele num: 65612
num of homozygotes: 0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.748e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.122999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

DP
type: SiteQuality
SIO_000300: 1.492606e6

VQSLOD
type: SiteQuality
SIO_000300: -1.094e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65440
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.347594261774788e-5
allele num: 15754
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.47759e6

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.281e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
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allele frequency: 6.485925541574782e-5
allele num: 15418
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64904
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.805e0

MQRankSum
type: SiteQuality
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele count: 0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.542495758136665e-5
allele num: 64830
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6570
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Other
type: Population
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allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180358829084042e-4
allele num: 8472
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 1.294911e6

FS
type: SiteQuality
SIO_000300: 1.688e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

GenotypeQuality
all individuals: 520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5622
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1926
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14752
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63958
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.316008316008316e-4
allele num: 9620
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.655e0

QD
type: SiteQuality
SIO_000300: 1.1e1

DP
type: SiteQuality
SIO_000300: 1.273201e6

FS
type: SiteQuality
SIO_000300: 1.6397e1

VQSLOD
type: SiteQuality
SIO_000300: -1.062e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 433
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7769
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14144
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4199
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578233010321644e-5
allele num: 63362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14438
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.862105636299185e-5
allele num: 11284
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.237976e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.46e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

GenotypeQuality
all individuals: 4404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5941
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

DP
type: SiteQuality
SIO_000300: 2.148666e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.437e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

FS
type: SiteQuality
SIO_000300: 5.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

GenotypeQuality
all individuals: 701
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.948304613674263e-5
allele num: 14392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.726e0

MQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.429e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 1.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

DP
type: SiteQuality
SIO_000300: 2.152395e6

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-5
allele num: 66080
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 2.246e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.369e0

QD
type: SiteQuality
SIO_000300: 9.73e0

DP
type: SiteQuality
SIO_000300: 2.158573e6

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

GenotypeQuality
all individuals: 4410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19096
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.714e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.26e-1

DP
type: SiteQuality
SIO_000300: 2.193915e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.437e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.573e0

FS
type: SiteQuality
SIO_000300: 4.081e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
all individuals: 2378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19098
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.321e1

MQ
type: SiteQuality
SIO_000300: 5.998e1

FS
type: SiteQuality
SIO_000300: 2.506e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

DP
type: SiteQuality
SIO_000300: 2.194321e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4407
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.195552e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

MQRankSum
type: SiteQuality
SIO_000300: 8.27e-1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3547
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4406
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4795
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19096
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99880023995201e-5
allele num: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.77e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

FS
type: SiteQuality
SIO_000300: 1.264e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

DP
type: SiteQuality
SIO_000300: 2.196551e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.071e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4793
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19092
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.463e-1

FS
type: SiteQuality
SIO_000300: 6.588e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.53e-1

QD
type: SiteQuality
SIO_000300: 9.56e0

DP
type: SiteQuality
SIO_000300: 2.196631e6

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.864e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.138e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.26e-1

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19088
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4405
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6169
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.331e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

FS
type: SiteQuality
SIO_000300: 1.2167e1

QD
type: SiteQuality
SIO_000300: 7.59e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 2.197428e6

GenotypeQuality
all individuals: 19087
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4794
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.197586e6

FS
type: SiteQuality
SIO_000300: 2.351e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.771e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

GenotypeQuality
all individuals: 17112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.349e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

FS
type: SiteQuality
SIO_000300: 5.133e0

DP
type: SiteQuality
SIO_000300: 2.197504e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.146e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 6178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.197279e6

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.479e0

VQSLOD
type: SiteQuality
SIO_000300: -2.293e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.76e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

GenotypeQuality
all individuals: 4395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17126
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19082
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 4773
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496402877697842e-5
allele num: 66720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.337e0

DP
type: SiteQuality
SIO_000300: 2.197167e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

FS
type: SiteQuality
SIO_000300: 2.599e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19077
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.823264859608606e-4
allele num: 16454
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0