1-3774129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774129
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774129
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 23338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16886
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30697
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

1-3774130-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774130
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774130
    reference: chr 1
allele count: 9491
allele frequency: 3.335793617320399e-1
allele num: 28452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.25e1
  variant carriers: 221
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 30725
  bin: 7.5e0
  variant carriers: 11732
genotype depth: GenotypeDepth
  all individuals: 10542
  bin: 1.25e1
  variant carriers: 5813
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.75e1
  variant carriers: 1135
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 13210
  bin: 2.5e0
  variant carriers: 2378
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 3.25e1
  variant carriers: 730
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.75e1
  variant carriers: 292
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 6.25e1
  variant carriers: 270
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 2.75e1
  variant carriers: 463
num of homozygotes: 1284
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

1-3774130-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774130
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774130
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 28452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-38A>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30725
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5641
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

1-3774133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774133
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774133
    reference: chr 1
allele count: 4
allele frequency: 1.365747063643813e-4
allele num: 29288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-35G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31281
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5495
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-3774134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774134
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774134
    reference: chr 1
allele count: 2
allele frequency: 6.793016778751444e-5
allele num: 29442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-34C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10547
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-3774137-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774137
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774137
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 29968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-31G>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12589
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10443
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

1-3774138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774138
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774138
    reference: chr 1
allele count: 13042
allele frequency: 3.689809313642279e-1
allele num: 35346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-30T>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 2.5e0
  variant carriers: 1123
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.75e1
  variant carriers: 2128
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 298
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 12826
  bin: 1.25e1
  variant carriers: 7670
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 30580
  bin: 7.5e0
  variant carriers: 9883
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.25e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 3.25e1
  variant carriers: 729
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 3.75e1
  variant carriers: 468
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 275
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 293
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 6.75e1
  variant carriers: 118
num of homozygotes: 1777
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

1-3774141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774141
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774141
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 37020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31254
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24837
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8526
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-3774157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774157
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774157
    reference: chr 1
allele count: 1
allele frequency: 2.303404431750127e-5
allele num: 43414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-11G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7261
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4847
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-3774161-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774161
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774161
    reference: chr 1
allele count: 2
allele frequency: 4.227793514564748e-5
allele num: 47306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-7A>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9994
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32511
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10304
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-3774162-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774162
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774162
    reference: chr 1
allele count: 2
allele frequency: 4.174668113884946e-5
allele num: 47908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.-6T>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9810
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3645
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/1-3774171-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774171
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774171
    reference: chr 1
allele count: 1
allele frequency: 1.795074316076686e-5
allele num: 55708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.4C>A
  hgvsp: ENSP00000367457.2:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.4C>A
  hgvsp: ENSP00000367454.3:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.4C>A
  hgvsp: ENSP00000462175.1:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.4C>A
  hgvsp: ENSP00000367448.1:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.4C>A
  hgvsp: ENSP00000436775.1:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.4C>A
  hgvsp: ENSP00000463688.1:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.4C>A
  hgvsp: ENSP00000463704.1:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.4C>A
  hgvsp: ENSP00000345906.3:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.4C>A
  hgvsp: ENSP00000339524.3:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.4C>A
  hgvsp: ENSP00000343218.3:p.Leu2Ile
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16128
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu2Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

1-3774173-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774173
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774173
    reference: chr 1
allele count: 1
allele frequency: 1.737196859148079e-5
allele num: 57564
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.6C>G
  hgvsp: ENST00000378209.3:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.6C>G
  hgvsp: ENST00000341385.3:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.6C>G
  hgvsp: ENST00000477548.1:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.6C>G
  hgvsp: ENST00000338895.3:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.6C>G
  hgvsp: ENST00000378206.1:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.6C>G
  hgvsp: ENST00000491998.1:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.6C>G
  hgvsp: ENST00000339350.3:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.6C>G
  hgvsp: ENST00000378212.2:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.6C>G
  hgvsp: ENST00000475969.1:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.6C>G
  hgvsp: ENST00000468793.1:c.6C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu2Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

1-3774179-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774179
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774179
    reference: chr 1
allele count: 2
allele frequency: 3.176014736708378e-5
allele num: 62972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.12G>T
  hgvsp: ENSP00000463688.1:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.12G>T
  hgvsp: ENSP00000343218.3:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.12G>T
  hgvsp: ENSP00000463704.1:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.12G>T
  hgvsp: ENSP00000436775.1:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.12G>T
  hgvsp: ENSP00000345906.3:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.12G>T
  hgvsp: ENSP00000339524.3:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.12G>T
  hgvsp: ENSP00000367448.1:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.12G>T
  hgvsp: ENSP00000367454.3:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.12G>T
  hgvsp: ENSP00000462175.1:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.12G>T
  hgvsp: ENSP00000367457.2:p.Lys4Asn
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20923
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys4Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/1-3774195-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774195
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774195
    reference: chr 1
allele count: 1
allele frequency: 1.433979580130779e-5
allele num: 69736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.28C>A
  hgvsp: ENSP00000436775.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.28C>A
  hgvsp: ENSP00000463704.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.28C>A
  hgvsp: ENSP00000367448.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.28C>A
  hgvsp: ENSP00000339524.3:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.28C>A
  hgvsp: ENSP00000367457.2:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.28C>A
  hgvsp: ENSP00000343218.3:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.28C>A
  hgvsp: ENSP00000367454.3:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.28C>A
  hgvsp: ENSP00000345906.3:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.28C>A
  hgvsp: ENSP00000462175.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.28C>A
  hgvsp: ENSP00000463688.1:p.Leu10Met
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu10Met
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: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

1-3774201-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774201
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774201
    reference: chr 1
allele count: 1
allele frequency: 1.422839418343246e-5
allele num: 70282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.34G>C
  hgvsp: ENSP00000367448.1:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.34G>C
  hgvsp: ENSP00000343218.3:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.34G>C
  hgvsp: ENSP00000345906.3:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.34G>C
  hgvsp: ENSP00000463704.1:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.34G>C
  hgvsp: ENSP00000463688.1:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.34G>C
  hgvsp: ENSP00000436775.1:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.34G>C
  hgvsp: ENSP00000339524.3:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.34G>C
  hgvsp: ENSP00000367457.2:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.34G>C
  hgvsp: ENSP00000367454.3:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.34G>C
  hgvsp: ENSP00000462175.1:p.Ala12Pro
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala12Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-3774212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774212
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774212
    reference: chr 1
allele count: 1
allele frequency: 1.422556048708319e-5
allele num: 70296
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.45C>T
  hgvsp: ENST00000378209.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.45C>T
  hgvsp: ENST00000491998.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.45C>T
  hgvsp: ENST00000339350.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.45C>T
  hgvsp: ENST00000378212.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.45C>T
  hgvsp: ENST00000378206.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.45C>T
  hgvsp: ENST00000468793.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.45C>T
  hgvsp: ENST00000475969.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.45C>T
  hgvsp: ENST00000338895.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.45C>T
  hgvsp: ENST00000341385.3:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.45C>T
  hgvsp: ENST00000477548.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser15Ser
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

1-3774221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774221
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774221
    reference: chr 1
allele count: 1
allele frequency: 1.513912859175826e-5
allele num: 66054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.54G>A
  hgvsp: ENST00000475969.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.54G>A
  hgvsp: ENST00000477548.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.54G>A
  hgvsp: ENST00000339350.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.54G>A
  hgvsp: ENST00000338895.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.54G>A
  hgvsp: ENST00000378212.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.54G>A
  hgvsp: ENST00000378209.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.54G>A
  hgvsp: ENST00000378206.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.54G>A
  hgvsp: ENST00000491998.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.54G>A
  hgvsp: ENST00000468793.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.54G>A
  hgvsp: ENST00000341385.3:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys18Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-3774221-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774221
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774221
    reference: chr 1
allele count: 2
allele frequency: 3.027825718351652e-5
allele num: 66054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.54G>T
  hgvsp: ENSP00000463704.1:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.54G>T
  hgvsp: ENSP00000343218.3:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.54G>T
  hgvsp: ENSP00000463688.1:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.54G>T
  hgvsp: ENSP00000367454.3:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.54G>T
  hgvsp: ENSP00000367448.1:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.54G>T
  hgvsp: ENSP00000367457.2:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.54G>T
  hgvsp: ENSP00000339524.3:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.54G>T
  hgvsp: ENSP00000462175.1:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.54G>T
  hgvsp: ENSP00000436775.1:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.54G>T
  hgvsp: ENSP00000345906.3:p.Lys18Asn
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10362
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys18Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

1-3774222-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774222
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774222
    reference: chr 1
allele count: 1
allele frequency: 1.512081531436175e-5
allele num: 66134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.55T>C
  hgvsp: ENSP00000436775.1:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.55T>C
  hgvsp: ENSP00000367457.2:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.55T>C
  hgvsp: ENSP00000345906.3:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.55T>C
  hgvsp: ENSP00000367454.3:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.55T>C
  hgvsp: ENSP00000463688.1:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.55T>C
  hgvsp: ENSP00000343218.3:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.55T>C
  hgvsp: ENSP00000463704.1:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.55T>C
  hgvsp: ENSP00000339524.3:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.55T>C
  hgvsp: ENSP00000367448.1:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.55T>C
  hgvsp: ENSP00000462175.1:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe19Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

1-3774226-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774226
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774226
    reference: chr 1
allele count: 1
allele frequency: 1.587553579933323e-5
allele num: 62990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.59G>C
  hgvsp: ENSP00000345906.3:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.59G>C
  hgvsp: ENSP00000436775.1:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.59G>C
  hgvsp: ENSP00000367457.2:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.59G>C
  hgvsp: ENSP00000339524.3:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.59G>C
  hgvsp: ENSP00000463704.1:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.59G>C
  hgvsp: ENSP00000343218.3:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.59G>C
  hgvsp: ENSP00000463688.1:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.59G>C
  hgvsp: ENSP00000367448.1:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.59G>C
  hgvsp: ENSP00000367454.3:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.59G>C
  hgvsp: ENSP00000462175.1:p.Gly20Ala
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly20Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

1-3774227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774227
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774227
    reference: chr 1
allele count: 1
allele frequency: 1.627392266631949e-5
allele num: 61448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.60C>T
  hgvsp: ENST00000339350.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.60C>T
  hgvsp: ENST00000491998.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.60C>T
  hgvsp: ENST00000477548.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.60C>T
  hgvsp: ENST00000378209.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.60C>T
  hgvsp: ENST00000378206.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.60C>T
  hgvsp: ENST00000378212.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.60C>T
  hgvsp: ENST00000338895.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.60C>T
  hgvsp: ENST00000341385.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.60C>T
  hgvsp: ENST00000475969.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.60C>T
  hgvsp: ENST00000468793.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly20Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-3774229-T-TGGCTGGCCGGAGCTGCCAGGAGGTGCTGCGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774229
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774260
    reference: chr 1
allele count: 1
allele frequency: 1.616658044490429e-5
allele num: 61856
alternate allele: TGGCTGGCCGGAGCTGCCAGGAGGTGCTGCGC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsp: ENSP00000345906.3:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsp: ENSP00000367448.1:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsp: ENSP00000339524.3:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsp: ENSP00000436775.1:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsp: ENSP00000463704.1:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsp: ENSP00000367457.2:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsp: ENSP00000343218.3:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsp: ENSP00000367454.3:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsp: ENSP00000462175.1:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsp: ENSP00000463688.1:p.Lys32GlyfsTer20
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 25139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12665
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32163
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys32GlyfsTer20
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

1-3774230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774230
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774230
    reference: chr 1
allele count: 1
allele frequency: 1.636607639684462e-5
allele num: 61102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.63G>A
  hgvsp: ENST00000339350.3:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.63G>A
  hgvsp: ENST00000491998.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.63G>A
  hgvsp: ENST00000338895.3:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.63G>A
  hgvsp: ENST00000341385.3:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.63G>A
  hgvsp: ENST00000378206.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.63G>A
  hgvsp: ENST00000468793.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.63G>A
  hgvsp: ENST00000378212.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.63G>A
  hgvsp: ENST00000477548.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.63G>A
  hgvsp: ENST00000475969.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.63G>A
  hgvsp: ENST00000378209.3:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10324
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val21Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-3774231-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774231
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774231
    reference: chr 1
allele count: 1
allele frequency: 1.734124093920161e-5
allele num: 57666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.64G>T
  hgvsp: ENSP00000367448.1:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.64G>T
  hgvsp: ENSP00000436775.1:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.64G>T
  hgvsp: ENSP00000345906.3:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.64G>T
  hgvsp: ENSP00000463704.1:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.64G>T
  hgvsp: ENSP00000367454.3:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.64G>T
  hgvsp: ENSP00000367457.2:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.64G>T
  hgvsp: ENSP00000339524.3:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.64G>T
  hgvsp: ENSP00000462175.1:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.64G>T
  hgvsp: ENSP00000463688.1:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.64G>T
  hgvsp: ENSP00000343218.3:p.Ala22Ser
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala22Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-3774239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774239
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774239
    reference: chr 1
allele count: 2
allele frequency: 3.712090278035562e-5
allele num: 53878
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.72G>A
  hgvsp: ENST00000378209.3:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.72G>A
  hgvsp: ENST00000468793.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.72G>A
  hgvsp: ENST00000475969.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.72G>A
  hgvsp: ENST00000339350.3:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.72G>A
  hgvsp: ENST00000477548.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.72G>A
  hgvsp: ENST00000378212.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.72G>A
  hgvsp: ENST00000378206.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.72G>A
  hgvsp: ENST00000491998.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.72G>A
  hgvsp: ENST00000341385.3:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.72G>A
  hgvsp: ENST00000338895.3:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26894
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15348
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-3774242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774242
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774242
    reference: chr 1
allele count: 1
allele frequency: 1.860949828792616e-5
allele num: 53736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.75C>T
  hgvsp: ENST00000339350.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.75C>T
  hgvsp: ENST00000475969.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.75C>T
  hgvsp: ENST00000378206.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.75C>T
  hgvsp: ENST00000468793.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.75C>T
  hgvsp: ENST00000338895.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.75C>T
  hgvsp: ENST00000378209.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.75C>T
  hgvsp: ENST00000477548.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.75C>T
  hgvsp: ENST00000378212.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.75C>T
  hgvsp: ENST00000341385.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.75C>T
  hgvsp: ENST00000491998.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15307
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser25Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

1-3774245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774245
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774245
    reference: chr 1
allele count: 1
allele frequency: 1.960323061240492e-5
allele num: 51012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.78C>T
  hgvsp: ENST00000378212.2:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.78C>T
  hgvsp: ENST00000338895.3:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.78C>T
  hgvsp: ENST00000468793.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.78C>T
  hgvsp: ENST00000339350.3:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.78C>T
  hgvsp: ENST00000491998.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.78C>T
  hgvsp: ENST00000475969.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.78C>T
  hgvsp: ENST00000378206.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.78C>T
  hgvsp: ENST00000378209.3:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.78C>T
  hgvsp: ENST00000341385.3:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.78C>T
  hgvsp: ENST00000477548.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys26Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-3774251-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774251
    reference: chr 1
allele count: 1
allele frequency: 2.071594298972489e-5
allele num: 48272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.84G>A
  hgvsp: ENST00000341385.3:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.84G>A
  hgvsp: ENST00000378212.2:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.84G>A
  hgvsp: ENST00000338895.3:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.84G>A
  hgvsp: ENST00000378209.3:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.84G>A
  hgvsp: ENST00000339350.3:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.84G>A
  hgvsp: ENST00000475969.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.84G>A
  hgvsp: ENST00000491998.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.84G>A
  hgvsp: ENST00000477548.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.84G>A
  hgvsp: ENST00000378206.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.84G>A
  hgvsp: ENST00000468793.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu28Glu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

1-3774253-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774253
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774253
    reference: chr 1
allele count: 1
allele frequency: 2.111308166539988e-5
allele num: 47364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.86T>G
  hgvsp: ENSP00000345906.3:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.86T>G
  hgvsp: ENSP00000367448.1:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.86T>G
  hgvsp: ENSP00000436775.1:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.86T>G
  hgvsp: ENSP00000463704.1:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.86T>G
  hgvsp: ENSP00000343218.3:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.86T>G
  hgvsp: ENSP00000463688.1:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.86T>G
  hgvsp: ENSP00000462175.1:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.86T>G
  hgvsp: ENSP00000367457.2:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.86T>G
  hgvsp: ENSP00000339524.3:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.86T>G
  hgvsp: ENSP00000367454.3:p.Val29Gly
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val29Gly
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

1-3774257-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774257
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774258
    reference: chr 1
allele count: 1
allele frequency: 2.219558751720158e-5
allele num: 45054
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.91dupC
  hgvsp: ENSP00000463704.1:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.91dupC
  hgvsp: ENSP00000367457.2:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.91dupC
  hgvsp: ENSP00000436775.1:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.91dupC
  hgvsp: ENSP00000463688.1:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.91dupC
  hgvsp: ENSP00000462175.1:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.91dupC
  hgvsp: ENSP00000339524.3:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.91dupC
  hgvsp: ENSP00000343218.3:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.91dupC
  hgvsp: ENSP00000367448.1:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.91dupC
  hgvsp: ENSP00000367454.3:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.91dupC
  hgvsp: ENSP00000345906.3:p.Arg31ProfsTer11
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg31ProfsTer11
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

1-3774258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774258
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774258
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 44276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.91C>T
  hgvsp: ENSP00000339524.3:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.91C>T
  hgvsp: ENSP00000463704.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.91C>T
  hgvsp: ENSP00000343218.3:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.91C>T
  hgvsp: ENSP00000463688.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.91C>T
  hgvsp: ENSP00000367457.2:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.91C>T
  hgvsp: ENSP00000367454.3:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.91C>T
  hgvsp: ENSP00000367448.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.91C>T
  hgvsp: ENSP00000462175.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.91C>T
  hgvsp: ENSP00000345906.3:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.91C>T
  hgvsp: ENSP00000436775.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27921
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg31Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-3774259-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774259
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774259
    reference: chr 1
allele count: 1
allele frequency: 2.285296402943462e-5
allele num: 43758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.92G>T
  hgvsp: ENSP00000367457.2:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.92G>T
  hgvsp: ENSP00000367448.1:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.92G>T
  hgvsp: ENSP00000462175.1:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.92G>T
  hgvsp: ENSP00000463688.1:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.92G>T
  hgvsp: ENSP00000367454.3:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.92G>T
  hgvsp: ENSP00000339524.3:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.92G>T
  hgvsp: ENSP00000343218.3:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.92G>T
  hgvsp: ENSP00000463704.1:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.92G>T
  hgvsp: ENSP00000436775.1:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.92G>T
  hgvsp: ENSP00000345906.3:p.Arg31Leu
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg31Leu
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: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-3774268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774268
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774268
    reference: chr 1
allele count: 1
allele frequency: 2.538715410002539e-5
allele num: 39390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.101G>A
  hgvsp: ENSP00000339524.3:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.101G>A
  hgvsp: ENSP00000367454.3:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.101G>A
  hgvsp: ENSP00000367457.2:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.101G>A
  hgvsp: ENSP00000367448.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.101G>A
  hgvsp: ENSP00000462175.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.101G>A
  hgvsp: ENSP00000345906.3:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.101G>A
  hgvsp: ENSP00000343218.3:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.101G>A
  hgvsp: ENSP00000436775.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.101G>A
  hgvsp: ENSP00000463688.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.101G>A
  hgvsp: ENSP00000463704.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys34Tyr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-3774274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774274
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774274
    reference: chr 1
allele count: 1
allele frequency: 2.847866947656206e-5
allele num: 35114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.107G>A
  hgvsp: ENSP00000367448.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.107G>A
  hgvsp: ENSP00000462175.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.107G>A
  hgvsp: ENSP00000343218.3:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.107G>A
  hgvsp: ENSP00000463704.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.107G>A
  hgvsp: ENSP00000339524.3:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.107G>A
  hgvsp: ENSP00000367457.2:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.107G>A
  hgvsp: ENSP00000367454.3:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.107G>A
  hgvsp: ENSP00000436775.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.107G>A
  hgvsp: ENSP00000345906.3:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.107G>A
  hgvsp: ENSP00000463688.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg36His
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-3774275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774275
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774275
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 35146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.108C>T
  hgvsp: ENST00000378212.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.108C>T
  hgvsp: ENST00000339350.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.108C>T
  hgvsp: ENST00000491998.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.108C>T
  hgvsp: ENST00000341385.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.108C>T
  hgvsp: ENST00000338895.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.108C>T
  hgvsp: ENST00000378206.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.108C>T
  hgvsp: ENST00000468793.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.108C>T
  hgvsp: ENST00000378209.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.108C>T
  hgvsp: ENST00000475969.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.108C>T
  hgvsp: ENST00000477548.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27215
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg36Arg
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-3774284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774284
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774284
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 30064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+3G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26878
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.114+3G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

1-3774285-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774285
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774285
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 30038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+4C>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26900
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.114+4C>G
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/1-3774286-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774286
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774286
    reference: chr 1
allele count: 1
allele frequency: 3.389141191622043e-5
allele num: 29506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+5C>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26892
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.114+5C>A
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-3774287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774287
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774287
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 28558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+6C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.114+6C>T
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

1-3774293-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774293
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774293
    reference: chr 1
allele count: 4
allele frequency: 1.631055292774425e-4
allele num: 24524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+12G>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26526
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6491
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-3774296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774296
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774296
    reference: chr 1
allele count: 8847
allele frequency: 3.633861825351187e-1
allele num: 24346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+15A>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 17467
  bin: 2.5e0
  variant carriers: 2127
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 25765
  bin: 7.5e0
  variant carriers: 10125
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.75e1
  variant carriers: 1269
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.25e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10187
  bin: 1.25e1
  variant carriers: 5764
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 12664
  bin: 2.25e1
  variant carriers: 1555
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 4.75e1
  variant carriers: 519
num of homozygotes: 1236
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-3774299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774299
    reference: chr 1
allele count: 1
allele frequency: 5.540780141843971e-5
allele num: 18048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+18C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24620
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7685
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

1-3774312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774312
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774312
    reference: chr 1
allele count: 5135
allele frequency: 3.600981767180926e-1
allele num: 14260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+31T>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22595
  bin: 2.5e0
  variant carriers: 3063
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 528
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 1.25e1
  variant carriers: 3482
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24067
  bin: 7.5e0
  variant carriers: 10551
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.25e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 8.75e1
  variant carriers: 856
genotype quality: GenotypeQuality
  all individuals: 17850
  bin: 7.5e0
  variant carriers: 940
num of homozygotes: 730
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

1-3774320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774320
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774320
    reference: chr 1
allele count: 1
allele frequency: 1.192748091603053e-4
allele num: 8384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+39G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30111
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-3774321-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774321
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774321
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 8038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+40C>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31413
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

1-3774328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3774328
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3774328
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 6504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.114+47G>A
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20224
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26957
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

1-3775236-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775236
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775236
    reference: chr 1
allele count: 2
allele frequency: 1.689931388785615e-5
allele num: 118348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-46C>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

1-3775237-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775237
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775237
    reference: chr 1
allele count: 1
allele frequency: 8.441953130276222e-6
allele num: 118456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-45G>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8429
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

1-3775242-G-GATGCAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775242
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775248
    reference: chr 1
allele count: 1
allele frequency: 8.431845393682861e-6
allele num: 118598
alternate allele: GATGCAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-39_115-38insTGCAAA
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-3775244-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775244
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775244
    reference: chr 1
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-38G>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-3775244-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775244
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775243
    reference: chr 1
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-37delA
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
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: GA
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

1-3775247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775247
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775247
    reference: chr 1
allele count: 1
allele frequency: 8.421052631578947e-6
allele num: 118750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-35C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

1-3775250-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775250
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775250
    reference: chr 1
allele count: 1
allele frequency: 8.408590215764425e-6
allele num: 118926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-32T>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8562
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-3775252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775252
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775252
    reference: chr 1
allele count: 2
allele frequency: 1.680644022789533e-5
allele num: 119002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-30C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-3775254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775254
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775254
    reference: chr 1
allele count: 7
allele frequency: 5.873961567508601e-5
allele num: 119170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-28C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14108
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

1-3775261-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775261
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775261
    reference: chr 1
allele count: 1
allele frequency: 8.366660531115611e-6
allele num: 119522
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-21T>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8683
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3456
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

1-3775271-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775271
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775271
    reference: chr 1
allele count: 1
allele frequency: 8.331111703545721e-6
allele num: 120032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-11C>G
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8929
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

1-3775272-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775272
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775272
    reference: chr 1
allele count: 107
allele frequency: 8.901089759587389e-4
allele num: 120210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-10G>C
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14237
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14438
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-3775276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775276
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775276
    reference: chr 1
allele count: 2
allele frequency: 1.661930165694438e-5
allele num: 120342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.115-6C>T
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-3775292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775292
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775292
    reference: chr 1
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.125G>A
  hgvsp: ENSP00000436775.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.125G>A
  hgvsp: ENSP00000345906.3:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.125G>A
  hgvsp: ENSP00000463704.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.125G>A
  hgvsp: ENSP00000367448.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.125G>A
  hgvsp: ENSP00000367457.2:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.125G>A
  hgvsp: ENSP00000339524.3:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.125G>A
  hgvsp: ENSP00000343218.3:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.125G>A
  hgvsp: ENSP00000367454.3:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.125G>A
  hgvsp: ENSP00000463688.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.125G>A
  hgvsp: ENSP00000462175.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg42His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

1-3775298-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775298
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775298
    reference: chr 1
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.131C>G
  hgvsp: ENSP00000436775.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.131C>G
  hgvsp: ENSP00000345906.3:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.131C>G
  hgvsp: ENSP00000343218.3:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.131C>G
  hgvsp: ENSP00000367457.2:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.131C>G
  hgvsp: ENSP00000339524.3:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.131C>G
  hgvsp: ENSP00000367448.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.131C>G
  hgvsp: ENSP00000463704.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.131C>G
  hgvsp: ENSP00000463688.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.131C>G
  hgvsp: ENSP00000367454.3:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.131C>G
  hgvsp: ENSP00000462175.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser44Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-3775299-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775299
    reference: chr 1
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.132C>A
  hgvsp: ENST00000378212.2:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.132C>A
  hgvsp: ENST00000341385.3:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.132C>A
  hgvsp: ENST00000378206.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.132C>A
  hgvsp: ENST00000339350.3:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.132C>A
  hgvsp: ENST00000475969.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.132C>A
  hgvsp: ENST00000338895.3:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.132C>A
  hgvsp: ENST00000491998.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.132C>A
  hgvsp: ENST00000477548.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.132C>A
  hgvsp: ENST00000468793.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.132C>A
  hgvsp: ENST00000378209.3:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser44Ser
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-3775313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775313
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775313
    reference: chr 1
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.146A>G
  hgvsp: ENSP00000343218.3:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.146A>G
  hgvsp: ENSP00000367448.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.146A>G
  hgvsp: ENSP00000339524.3:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.146A>G
  hgvsp: ENSP00000463704.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.146A>G
  hgvsp: ENSP00000367454.3:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.146A>G
  hgvsp: ENSP00000462175.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.146A>G
  hgvsp: ENSP00000367457.2:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.146A>G
  hgvsp: ENSP00000345906.3:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.146A>G
  hgvsp: ENSP00000436775.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.146A>G
  hgvsp: ENSP00000463688.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr49Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-3775314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775314
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775314
    reference: chr 1
allele count: 13
allele frequency: 1.072943662204321e-4
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.147C>T
  hgvsp: ENST00000468793.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.147C>T
  hgvsp: ENST00000338895.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.147C>T
  hgvsp: ENST00000341385.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.147C>T
  hgvsp: ENST00000339350.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.147C>T
  hgvsp: ENST00000378209.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.147C>T
  hgvsp: ENST00000475969.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.147C>T
  hgvsp: ENST00000378206.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.147C>T
  hgvsp: ENST00000378212.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.147C>T
  hgvsp: ENST00000491998.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.147C>T
  hgvsp: ENST00000477548.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr49Tyr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/1-3775316-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775316
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.149A>C
  hgvsp: ENSP00000367448.1:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.149A>C
  hgvsp: ENSP00000343218.3:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.149A>C
  hgvsp: ENSP00000339524.3:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.149A>C
  hgvsp: ENSP00000463688.1:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.149A>C
  hgvsp: ENSP00000436775.1:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.149A>C
  hgvsp: ENSP00000462175.1:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.149A>C
  hgvsp: ENSP00000367454.3:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.149A>C
  hgvsp: ENSP00000463704.1:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.149A>C
  hgvsp: ENSP00000367457.2:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.149A>C
  hgvsp: ENSP00000345906.3:p.Glu50Ala
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu50Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

1-3775316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775316
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775316
    reference: chr 1
allele count: 26
allele frequency: 2.145851903205573e-4
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.149A>G
  hgvsp: ENSP00000436775.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.149A>G
  hgvsp: ENSP00000462175.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.149A>G
  hgvsp: ENSP00000343218.3:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.149A>G
  hgvsp: ENSP00000463688.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.149A>G
  hgvsp: ENSP00000339524.3:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.149A>G
  hgvsp: ENSP00000367457.2:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.149A>G
  hgvsp: ENSP00000367448.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.149A>G
  hgvsp: ENSP00000463704.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.149A>G
  hgvsp: ENSP00000345906.3:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.149A>G
  hgvsp: ENSP00000367454.3:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu50Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-3775326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775326
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775326
    reference: chr 1
allele count: 2
allele frequency: 1.651091371396493e-5
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.159G>A
  hgvsp: ENST00000491998.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.159G>A
  hgvsp: ENST00000339350.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.159G>A
  hgvsp: ENST00000338895.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.159G>A
  hgvsp: ENST00000475969.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.159G>A
  hgvsp: ENST00000468793.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.159G>A
  hgvsp: ENST00000477548.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.159G>A
  hgvsp: ENST00000378212.2:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.159G>A
  hgvsp: ENST00000341385.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.159G>A
  hgvsp: ENST00000378206.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.159G>A
  hgvsp: ENST00000378209.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr53Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-3775327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3775327
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 3775327
    reference: chr 1
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000339524
  ensembl transcript: ENST00000338895
  gene symbol: DFFB
  hgvsc: ENST00000338895.3:c.160G>A
  hgvsp: ENSP00000339524.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367448
  ensembl transcript: ENST00000378206
  gene symbol: DFFB
  hgvsc: ENST00000378206.1:c.160G>A
  hgvsp: ENSP00000367448.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000462175
  ensembl transcript: ENST00000477548
  gene symbol: DFFB
  hgvsc: ENST00000477548.1:c.160G>A
  hgvsp: ENSP00000462175.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000345906
  ensembl transcript: ENST00000341385
  gene symbol: DFFB
  hgvsc: ENST00000341385.3:c.160G>A
  hgvsp: ENSP00000345906.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463704
  ensembl transcript: ENST00000475969
  gene symbol: DFFB
  hgvsc: ENST00000475969.1:c.160G>A
  hgvsp: ENSP00000463704.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367454
  ensembl transcript: ENST00000378209
  gene symbol: DFFB
  hgvsc: ENST00000378209.3:c.160G>A
  hgvsp: ENSP00000367454.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000367457
  ensembl transcript: ENST00000378212
  gene symbol: DFFB
  hgvsc: ENST00000378212.2:c.160G>A
  hgvsp: ENSP00000367457.2:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000463688
  ensembl transcript: ENST00000468793
  gene symbol: DFFB
  hgvsc: ENST00000468793.1:c.160G>A
  hgvsp: ENSP00000463688.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000343218
  ensembl transcript: ENST00000339350
  gene symbol: DFFB
  hgvsc: ENST00000339350.3:c.160G>A
  hgvsp: ENSP00000343218.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169598
  ensembl protein: ENSP00000436775
  ensembl transcript: ENST00000491998
  gene symbol: DFFB
  hgvsc: ENST00000491998.1:c.160G>A
  hgvsp: ENSP00000436775.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/2773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu54Lys
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13623
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6068
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6285
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3312
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12866
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.43e-2

QD
type: SiteQuality
SIO_000300: 2.644e1

VQSLOD
type: SiteQuality
SIO_000300: -2.479e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 4.92622e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3468
bin: 1.75e1
variant carriers: 872

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 234

GenotypeQuality
all individuals: 456
bin: 4.75e1
variant carriers: 340

GenotypeQuality
all individuals: 1122
bin: 3.75e1
variant carriers: 469

GenotypeQuality
all individuals: 3463
bin: 1.25e1
variant carriers: 398

GenotypeQuality
all individuals: 7722
bin: 7.5e0
variant carriers: 290

GenotypeQuality
all individuals: 341
bin: 9.25e1
variant carriers: 327

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 126

GenotypeQuality
all individuals: 5641
bin: 2.5e0
variant carriers: 43

GenotypeQuality
all individuals: 446
bin: 4.25e1
variant carriers: 279

GenotypeQuality
all individuals: 13167
bin: 2.25e1
variant carriers: 1036

GenotypeQuality
all individuals: 311
bin: 6.75e1
variant carriers: 120

GenotypeQuality
all individuals: 189
bin: 8.25e1
variant carriers: 155

GenotypeQuality
all individuals: 15603
bin: 9.75e1
variant carriers: 15550

GenotypeQuality
all individuals: 327
bin: 5.25e1
variant carriers: 303

European (Finnish)
type: Population
allele count: 282
allele frequency: 3.455882352941176e-1
allele num: 816
num of homozygotes: 33

Other
type: Population
allele count: 67
allele frequency: 3.602150537634409e-1
allele num: 186
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 5139
allele frequency: 3.249241274658574e-1
allele num: 15816
num of homozygotes: 606

Latino
type: Population
allele count: 529
allele frequency: 2.834941050375134e-1
allele num: 1866
num of homozygotes: 46

African
type: Population
allele count: 1547
allele frequency: 4.719341061622941e-1
allele num: 3278
num of homozygotes: 334

South Asian
type: Population
allele count: 1541
allele frequency: 3.389793224813022e-1
allele num: 4546
num of homozygotes: 230

East Asian
type: Population
allele count: 386
allele frequency: 1.98559670781893e-1
allele num: 1944
num of homozygotes: 28

DP
type: SiteQuality
SIO_000300: 5.25961e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.198e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.555e1

GenotypeQuality
all individuals: 456
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13167
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7722
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15603
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1866
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.198e-1

QD
type: SiteQuality
SIO_000300: 2.555e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

DP
type: SiteQuality
SIO_000300: 5.25961e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

GenotypeQuality
all individuals: 4472
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1100
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6941
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10865
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 21253
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 1.483679525222552e-3
allele num: 2022
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.030181086519115e-4
allele num: 1988
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.397e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

DP
type: SiteQuality
SIO_000300: 5.31131e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

FS
type: SiteQuality
SIO_000300: 1.2623e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.33e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
all individuals: 242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2048
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 6.049606775559589e-4
allele num: 3306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.33617e5

MQ
type: SiteQuality
SIO_000300: 5.787e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.333e0

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.507e0

QD
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

GenotypeQuality
all individuals: 29
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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: 245
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.43631e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.397e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.746e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 305

GenotypeQuality
all individuals: 190
bin: 8.25e1
variant carriers: 156

GenotypeQuality
all individuals: 6662
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variant carriers: 290

GenotypeQuality
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variant carriers: 870

GenotypeQuality
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variant carriers: 43

GenotypeQuality
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bin: 1.25e1
variant carriers: 394

GenotypeQuality
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variant carriers: 327

GenotypeQuality
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variant carriers: 280

GenotypeQuality
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GenotypeQuality
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variant carriers: 1027

GenotypeQuality
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variant carriers: 239

GenotypeQuality
all individuals: 15586
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variant carriers: 15534

GenotypeQuality
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bin: 2.75e1
variant carriers: 460

GenotypeQuality
all individuals: 453
bin: 4.75e1
variant carriers: 337

GenotypeQuality
all individuals: 122
bin: 7.25e1
variant carriers: 70

European (Non-Finnish)
type: Population
allele count: 7135
allele frequency: 3.61412217607132e-1
allele num: 19742
num of homozygotes: 854

Latino
type: Population
allele count: 848
allele frequency: 3.375796178343949e-1
allele num: 2512
num of homozygotes: 75

East Asian
type: Population
allele count: 538
allele frequency: 2.301112061591103e-1
allele num: 2338
num of homozygotes: 43

South Asian
type: Population
allele count: 2065
allele frequency: 3.746371552975327e-1
allele num: 5512
num of homozygotes: 311

Other
type: Population
allele count: 83
allele frequency: 3.878504672897196e-1
allele num: 214
num of homozygotes: 9

African
type: Population
allele count: 1945
allele frequency: 4.987179487179487e-1
allele num: 3900
num of homozygotes: 436

European (Finnish)
type: Population
allele count: 428
allele frequency: 3.794326241134752e-1
allele num: 1128
num of homozygotes: 49

QD
type: SiteQuality
SIO_000300: 2.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.519999999999999e-2

DP
type: SiteQuality
SIO_000300: 5.83031e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 4137
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GenotypeQuality
all individuals: 423
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 4922
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GenotypeQuality
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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: 225
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 1012
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2480
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

QD
type: SiteQuality
SIO_000300: 1.525e1

VQSLOD
type: SiteQuality
SIO_000300: -2.802e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.4485e5

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 2141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 393
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GenotypeQuality
all individuals: 4279
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 82
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GenotypeQuality
all individuals: 225
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3350
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.532801961986511e-4
allele num: 6524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.793e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 2.379e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.282e0

VQSLOD
type: SiteQuality
SIO_000300: -2.182e0

DP
type: SiteQuality
SIO_000300: 6.4343e5

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3312
bin: 2.75e1
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GenotypeQuality
all individuals: 3935
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GenotypeQuality
all individuals: 885
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variant carriers: 0

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 173
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GenotypeQuality
all individuals: 716
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GenotypeQuality
all individuals: 32636
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GenotypeQuality
all individuals: 227
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variant carriers: 2

GenotypeQuality
all individuals: 693
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GenotypeQuality
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.531254707034192e-5
allele num: 26556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.067e0

QD
type: SiteQuality
SIO_000300: 1.151e1

VQSLOD
type: SiteQuality
SIO_000300: -7.25e-2

FS
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 6.84856e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 521
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.43549706297866e-5
allele num: 26898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3962
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.184e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.675e0

DP
type: SiteQuality
SIO_000300: 6.91932e5

GenotypeQuality
all individuals: 677
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
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GenotypeQuality
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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: 957
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 179
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GenotypeQuality
all individuals: 2776
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GenotypeQuality
all individuals: 2467
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GenotypeQuality
all individuals: 468
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GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 226
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GenotypeQuality
all individuals: 2433
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GenotypeQuality
all individuals: 555
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4942
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.222792858889704e-4
allele num: 8178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4874
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31336
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

FS
type: SiteQuality
SIO_000300: 3.796e0

DP
type: SiteQuality
SIO_000300: 7.81931e5

QD
type: SiteQuality
SIO_000300: 1.077e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

GenotypeQuality
all individuals: 100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.5e0
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GenotypeQuality
all individuals: 1028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1065
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29634
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 582
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.179801793298726e-4
allele num: 8476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5106
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.579e0

DP
type: SiteQuality
SIO_000300: 8.00966e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

QD
type: SiteQuality
SIO_000300: 2.727e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 146
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.07000407000407e-4
allele num: 4914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.22e-2

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

DP
type: SiteQuality
SIO_000300: 8.52035e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

QD
type: SiteQuality
SIO_000300: 7.17e0

GenotypeQuality
all individuals: 157
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24897
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variant carriers: 0

GenotypeQuality
all individuals: 1490
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 226
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variant carriers: 1

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2292
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10564
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.163e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.098e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.098e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.07797e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

GenotypeQuality
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 2500
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
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variant carriers: 0

GenotypeQuality
all individuals: 1417
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variant carriers: 0

GenotypeQuality
all individuals: 256
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variant carriers: 0

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 255
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1405
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.375585974123383e-5
allele num: 10666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

DP
type: SiteQuality
SIO_000300: 9.09159e5

VQSLOD
type: SiteQuality
SIO_000300: -1.413e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 4.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

GenotypeQuality
all individuals: 22386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 272
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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: 2730
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 1367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 225
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.573340195573855e-5
allele num: 38860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.246e0

VQSLOD
type: SiteQuality
SIO_000300: -2.578e0

QD
type: SiteQuality
SIO_000300: 4.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 2.06e0

DP
type: SiteQuality
SIO_000300: 9.01614e5

GenotypeQuality
all individuals: 447
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

South Asian
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: 6082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36428
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.864975755315181e-4
allele num: 5362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2228
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.849e0

DP
type: SiteQuality
SIO_000300: 8.36597e5

QD
type: SiteQuality
SIO_000300: 4.49e0

FS
type: SiteQuality
SIO_000300: 2.296e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

GenotypeQuality
all individuals: 699
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.490282200505106e-5
allele num: 36428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2228
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 4.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.849e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

FS
type: SiteQuality
SIO_000300: 2.296e0

DP
type: SiteQuality
SIO_000300: 8.36597e5

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: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 1.944012441679627e-4
allele num: 5144
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36486
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2220
num of homozygotes: 0

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

ClippingRankSum
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MQ
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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SIO_000300: 7.89e-1

VQSLOD
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FS
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InbreedingCoeff
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SIO_000300: -9.1e-3

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5690
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4874
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 34710
num of homozygotes: 0

South Asian
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allele frequency: 9.956192751891676e-5
allele num: 10044
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 2.109704641350211e-4
allele num: 4740
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.934788988671715e-5
allele num: 34074
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
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ClippingRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 5.287e1

InbreedingCoeff
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SIO_000300: -1.02e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.637e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 5500
num of homozygotes: 0

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

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

African
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allele frequency: 2.00160128102482e-4
allele num: 4996
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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DP
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SIO_000300: 7.65154e5

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 31676
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 9352
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European (Finnish)
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allele frequency: 0.0e0
allele num: 1850
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Latino
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East Asian
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Other
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MQ
type: SiteQuality
SIO_000300: 5.907e1

VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 29654
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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DP
type: SiteQuality
SIO_000300: 6.7795e5

MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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Latino
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East Asian
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South Asian
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European (Finnish)
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African
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Other
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ReadPosRankSum
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DP
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.46e-2

BaseQRankSum
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SIO_000300: -8.98e-1

MQ
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SIO_000300: 6.0e1

QD
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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allele frequency: 1.202790473899447e-4
allele num: 8314
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 28140
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.94e-1

MQRankSum
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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SIO_000300: -1.65e-2

ClippingRankSum
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SIO_000300: -1.658e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.747002398081535e-5
allele num: 26688
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1510
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DP
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SIO_000300: 6.14402e5

BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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SIO_000300: 5.884e1

ReadPosRankSum
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SIO_000300: -3.4e-1

VQSLOD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.820585313670054e-5
allele num: 26174
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 2.106e1

InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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FS
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VQSLOD
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7370
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 4.010909674314134e-5
allele num: 24932
num of homozygotes: 0

QD
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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MQ
type: SiteQuality
SIO_000300: 6.011e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 316
num of homozygotes: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 1.40805406927626e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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ClippingRankSum
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SIO_000300: 2.71e-1

InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 3.017501508750754e-4
allele num: 3314
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

MQRankSum
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 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
allele num: 3082
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.122011541632317e-4
allele num: 2426
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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ClippingRankSum
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SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.13e-2

QD
type: SiteQuality
SIO_000300: 5.84e0

MQRankSum
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SIO_000300: 1.82e0

DP
type: SiteQuality
SIO_000300: 4.96569e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3096
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 2442
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2884
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

MQRankSum
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -7.31e-1

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

South Asian
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allele frequency: 0.0e0
allele num: 4992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16940
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

MQRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2024
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4940
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16960
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.58186e5

QD
type: SiteQuality
SIO_000300: 2.692e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 5.096839959225281e-4
allele num: 1962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.897e0

VQSLOD
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.66e-2

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 4.5079e5

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2298
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.288629737609329e-5
allele num: 13720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 7.159904534606205e-4
allele num: 4190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.89e-2

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.127e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.27386e5

GenotypeQuality
all individuals: 757
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variant carriers: 751

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7310

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 778

South Asian
type: Population
allele count: 1496
allele frequency: 3.572110792741165e-1
allele num: 4188
num of homozygotes: 216

African
type: Population
allele count: 1212
allele frequency: 5.161839863713799e-1
allele num: 2348
num of homozygotes: 277

Latino
type: Population
allele count: 559
allele frequency: 3.172531214528944e-1
allele num: 1762
num of homozygotes: 53

Other
type: Population
allele count: 57
allele frequency: 3.392857142857143e-1
allele num: 168
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 282
allele frequency: 3.790322580645161e-1
allele num: 744
num of homozygotes: 32

European (Non-Finnish)
type: Population
allele count: 4887
allele frequency: 3.60132645541636e-1
allele num: 13570
num of homozygotes: 625

East Asian
type: Population
allele count: 354
allele frequency: 2.260536398467433e-1
allele num: 1566
num of homozygotes: 26

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 9.09e-1

QD
type: SiteQuality
SIO_000300: 1.916e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 4.23756e5

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 1477
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.162555344718533e-4
allele num: 3162
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.69e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

VQSLOD
type: SiteQuality
SIO_000300: -1.455e0

DP
type: SiteQuality
SIO_000300: 3.71264e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.038e1

MQ
type: SiteQuality
SIO_000300: 5.811e1

GenotypeQuality
all individuals: 310
bin: 7.25e1
variant carriers: 292

GenotypeQuality
all individuals: 865
bin: 9.25e1
variant carriers: 853

GenotypeQuality
all individuals: 1270
bin: 2.75e1
variant carriers: 847

GenotypeQuality
all individuals: 363
bin: 6.75e1
variant carriers: 303

GenotypeQuality
all individuals: 7116
bin: 2.5e0
variant carriers: 105

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 320

GenotypeQuality
all individuals: 3230
bin: 1.75e1
variant carriers: 1689

GenotypeQuality
all individuals: 1019
bin: 5.75e1
variant carriers: 1012

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 235

GenotypeQuality
all individuals: 870
bin: 6.25e1
variant carriers: 643

GenotypeQuality
all individuals: 792
bin: 5.25e1
variant carriers: 783

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 293

GenotypeQuality
all individuals: 447
bin: 4.75e1
variant carriers: 431

GenotypeQuality
all individuals: 3491
bin: 1.25e1
variant carriers: 886

GenotypeQuality
all individuals: 8310
bin: 2.25e1
variant carriers: 1503

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 601

GenotypeQuality
all individuals: 5017
bin: 9.75e1
variant carriers: 4969

GenotypeQuality
all individuals: 812
bin: 3.25e1
variant carriers: 527

Other
type: Population
allele count: 33
allele frequency: 3.3e-1
allele num: 100
num of homozygotes: 3

East Asian
type: Population
allele count: 197
allele frequency: 2.184035476718404e-1
allele num: 902
num of homozygotes: 14

European (Finnish)
type: Population
allele count: 158
allele frequency: 3.708920187793427e-1
allele num: 426
num of homozygotes: 17

African
type: Population
allele count: 768
allele frequency: 5.12e-1
allele num: 1500
num of homozygotes: 175

Latino
type: Population
allele count: 258
allele frequency: 3.265822784810127e-1
allele num: 790
num of homozygotes: 26

South Asian
type: Population
allele count: 953
allele frequency: 3.540118870728083e-1
allele num: 2692
num of homozygotes: 139

European (Non-Finnish)
type: Population
allele count: 2768
allele frequency: 3.526114649681529e-1
allele num: 7850
num of homozygotes: 356

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 1.297e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.005e1

DP
type: SiteQuality
SIO_000300: 3.4446e5

GenotypeQuality
all individuals: 78
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3868
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6621
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9716
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165228113440197e-4
allele num: 1622
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.23e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.599e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 2.83848e5

QD
type: SiteQuality
SIO_000300: 9.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6759
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29911
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

DP
type: SiteQuality
SIO_000300: 2.81465e5

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.39e-2

QD
type: SiteQuality
SIO_000300: 1.504e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6561
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7617
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5323
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6325
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.582e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 2.71425e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.950000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10589
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2950
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.040252949045361e-5
allele num: 65784
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: 14544
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: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 1.512e0

QD
type: SiteQuality
SIO_000300: 1.113e1

MQRankSum
type: SiteQuality
SIO_000300: -4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 2.04014e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 5135
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2947
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
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variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4278
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
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: 1.520034048762692e-5
allele num: 65788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.686e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

DP
type: SiteQuality
SIO_000300: 2.041558e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5148
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8453
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10587
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.794401413235494e-5
allele num: 14718
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

FS
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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QD
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.517865274278255e-5
allele num: 65882
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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QD
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DP
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.516990291262136e-5
allele num: 65920
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Latino
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Other
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South Asian
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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East Asian
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African
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Other
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European (Non-Finnish)
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QD
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
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

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

Other
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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ClippingRankSum
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FS
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.667e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66228
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

African
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allele frequency: 1.012536162005786e-2
allele num: 10370
num of homozygotes: 0

VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.4e-1

QD
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.156604210039325e-4
allele num: 8646
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66256
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Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
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FS
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QD
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 7.26e-1

ClippingRankSum
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SIO_000300: -8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

MQ
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SIO_000300: 5.929e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: 2.0e-4

QD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
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SIO_000300: -3.01e-1

VQSLOD
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SIO_000300: 4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

FS
type: SiteQuality
SIO_000300: 7.072e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66500
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 6.056201550387597e-5
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European (Finnish)
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allele frequency: 0.0e0
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African
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

Other
type: Population
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South Asian
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allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66534
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European (Finnish)
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Latino
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East Asian
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allele frequency: 8.098102730217492e-4
allele num: 8644
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22980
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10513
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5182
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 8644
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 2.096224e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5182
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2947
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10513
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 23
allele frequency: 1.392926356589147e-3
allele num: 16512
num of homozygotes: 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: 8644
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: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005710850616171e-5
allele num: 66540
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.286e1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

DP
type: SiteQuality
SIO_000300: 2.096224e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 225
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1898
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8870
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5176
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22907
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10485
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4293
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.094838e6

QD
type: SiteQuality
SIO_000300: 1.36e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

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

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5176
bin: 7.75e1
variant carriers: 0