6-31498183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498183
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498183
    reference: chr 6
allele count: 16
allele frequency: 1.381167777355754e-4
allele num: 115844
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1529G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*246G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.455G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3840G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*60G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.787G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7025
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-31498184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498184
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498184
    reference: chr 6
allele count: 3
allele frequency: 2.589153174301792e-5
allele num: 115868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.786C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3839C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1528C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*59C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.454C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*245C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8170
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-31498191-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498191
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498191
    reference: chr 6
allele count: 1
allele frequency: 8.625150940141453e-6
allele num: 115940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*238A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1521A>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3832A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*20A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*52A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*20A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*20A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*20A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.779A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.447A>G
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

6-31498200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498200
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498200
    reference: chr 6
allele count: 20
allele frequency: 1.724435247456458e-4
allele num: 115980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3823C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.770C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*43C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1512C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.438C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4515
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

6-31498202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498202
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498202
    reference: chr 6
allele count: 1
allele frequency: 8.620243780494112e-6
allele num: 116006
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1510C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.768C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.436C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*9C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*9C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*227C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3821C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

6-31498202-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498202
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498202
    reference: chr 6
allele count: 1
allele frequency: 8.620243780494112e-6
allele num: 116006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3821C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*9C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*9C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1510C>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.436C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*9C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.768C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*227C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*9C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*41C>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-31498203-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498203
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498203
    reference: chr 6
allele count: 1480
allele frequency: 1.275554176578067e-2
allele num: 116028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*8G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.435G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3820G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*8G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*8G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*226G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1509G>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*40G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.767G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*8G>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 6.75e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 5.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 4.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 2.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 5.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 7815
  bin: 3.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 4.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 6.25e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 30017
  bin: 9.75e1
  variant carriers: 1450
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 18
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

6-31498203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498203
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498203
    reference: chr 6
allele count: 11
allele frequency: 9.480470231323473e-5
allele num: 116028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.*8G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.*8G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.767G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.435G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.*8G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*40G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1509G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3820G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.*8G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7815
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

6-31498215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498215
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498215
    reference: chr 6
allele count: 1
allele frequency: 8.616232982939859e-6
allele num: 116060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.423G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1049G>A
  hgvsp: ENSP00000392669.2:p.Arg350Gln
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3808G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1497G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1283G>A
  hgvsp: ENSP00000379475.1:p.Arg428Gln
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*214G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1328G>A
  hgvsp: ENSP00000412582.2:p.Arg443Gln
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.755G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1283G>A
  hgvsp: ENSP00000416269.1:p.Arg428Gln
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg428Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-31498223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498223
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498223
    reference: chr 6
allele count: 1
allele frequency: 8.615342201392239e-6
allele num: 116072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*206A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1275A>G
  hgvsp: ENST00000458640.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1041A>G
  hgvsp: ENST00000415382.2:c.1041A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.747A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*20A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1320A>G
  hgvsp: ENST00000417556.2:c.1320A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3800A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.415A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1489A>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1275A>G
  hgvsp: ENST00000396172.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu425Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-31498234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498234
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498234
    reference: chr 6
allele count: 1
allele frequency: 8.658608388459807e-6
allele num: 115492
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-7T>C
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-7T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.404T>C
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3282
  bin: 9.25e1
  variant carriers: 0
hgvs: c.1271-7T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

6-31498241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498241
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498241
    reference: chr 6
allele count: 1
allele frequency: 8.688399249322305e-6
allele num: 115096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-14C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.397C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-14C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-14C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8037
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

6-31498244-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498244
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498245
    reference: chr 6
allele count: 9653
allele frequency: 8.318969974835395e-2
allele num: 116036
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.393dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-18dupG
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-18dupG
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-18dupG
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 335
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 4.25e1
  variant carriers: 657
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 6.25e1
  variant carriers: 768
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.25e1
  variant carriers: 321
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 2.75e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.75e1
  variant carriers: 561
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 2.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 4.75e1
  variant carriers: 750
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 6.75e1
  variant carriers: 688
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 5.75e1
  variant carriers: 838
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 9.75e1
  variant carriers: 1180
genotype depth: GenotypeDepth
  all individuals: 7177
  bin: 3.75e1
  variant carriers: 515
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 5.25e1
  variant carriers: 784
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 637
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 8.75e1
  variant carriers: 395
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 471
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

6-31498248-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498248
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498248
    reference: chr 6
allele count: 1
allele frequency: 8.617123948710878e-6
allele num: 116048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.390C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-21C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-21C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-21C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-31498253-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498253
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498253
    reference: chr 6
allele count: 1
allele frequency: 8.617272460920669e-6
allele num: 116046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.385C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-26C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-26C>G
  variant of: http://identifiers.org/hgnc/41999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3219
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-31498261-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498261
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498261
    reference: chr 6
allele count: 1
allele frequency: 8.619352169490942e-6
allele num: 116018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.377G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-34G>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-34G>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-34G>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

6-31498263-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498263
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498263
    reference: chr 6
allele count: 5
allele frequency: 4.308784750349012e-5
allele num: 116042
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-36A>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.375A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-36A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-36A>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-31498268-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498268
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498268
    reference: chr 6
allele count: 1
allele frequency: 8.619352169490942e-6
allele num: 116018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-41T>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.370T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-41T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-41T>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-31498275-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498275
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498275
    reference: chr 6
allele count: 1
allele frequency: 8.621135575978068e-6
allele num: 115994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.363T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*16-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1271-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*202-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.743-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1271-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1485-48T>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3796-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1316-48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1037-48T>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31672
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/6-31498506-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498506
    reference: chr 6
allele count: 4
allele frequency: 3.479713271626418e-5
allele num: 114952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.132T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+50T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+50T>G
  variant of: http://identifiers.org/hgnc/41999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2352
  bin: 8.75e1
  variant carriers: 0
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: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/6-31498508-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498508
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498508
    reference: chr 6
allele count: 1
allele frequency: 8.700191404210892e-6
allele num: 114940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+48T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.130T>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+48T>G
  variant of: http://identifiers.org/hgnc/41999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27772
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

6-31498510-T-TAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498510
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498513
    reference: chr 6
allele count: 1
allele frequency: 8.699131826643701e-6
allele num: 114954
alternate allele: TAAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+43_1036+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+43_*201+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+43_742+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.125_127dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+43_*1484+45dupCTT
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+43_1270+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+43_1270+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+43_*15+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+43_1315+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+43_3795+45dupCTT
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2356
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-31498512-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498512
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498513
    reference: chr 6
allele count: 1
allele frequency: 8.698526469616046e-6
allele num: 114962
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.125dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+43dupC
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+43dupC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+43dupC
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

6-31498512-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498512
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498512
    reference: chr 6
allele count: 1
allele frequency: 8.698526469616046e-6
allele num: 114962
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.126T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+44T>C
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+44T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+44T>C
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3659
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-31498513-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498513
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498513
    reference: chr 6
allele count: 1
allele frequency: 8.696710903936131e-6
allele num: 114986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.125C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+43C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+43C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+43C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

6-31498520-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498520
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498520
    reference: chr 6
allele count: 1
allele frequency: 8.686587908269631e-6
allele num: 115120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.118C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+36C>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+36C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+36C>A
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-31498523-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498523
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498523
    reference: chr 6
allele count: 1
allele frequency: 8.684023134237629e-6
allele num: 115154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+33C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.115C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+33C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+33C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7530
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-31498527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498527
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498527
    reference: chr 6
allele count: 1
allele frequency: 8.678144959733408e-6
allele num: 115232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+29G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-1G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+29G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+29G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 6.75e1
  variant carriers: 0
hgvs: n.112-1G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-31498532-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498532
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498532
    reference: chr 6
allele count: 1
allele frequency: 8.662058451570432e-6
allele num: 115446
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+24C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-6C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+24C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+24C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
hgvs: n.112-6C>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-31498532-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498532
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498532
    reference: chr 6
allele count: 1
allele frequency: 8.662058451570432e-6
allele num: 115446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-6C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+24C>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+24C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+24C>A
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
hgvs: n.112-6C>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-31498534-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498534
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498534
    reference: chr 6
allele count: 2
allele frequency: 1.731361889262094e-5
allele num: 115516
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+22C>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-8C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+22C>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+22C>A
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27794
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
hgvs: n.112-8C>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

6-31498535-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498535
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498535
    reference: chr 6
allele count: 1
allele frequency: 8.653962649497205e-6
allele num: 115554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+21A>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-9A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+21A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+21A>G
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27793
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

6-31498547-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498547
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498547
    reference: chr 6
allele count: 2
allele frequency: 1.726251100485076e-5
allele num: 115858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1315+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*15+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1270+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*201+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1484+9T>C
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-21T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.742+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3795+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1036+9T>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1270+9T>C
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3928
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-31498561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498561
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498561
    reference: chr 6
allele count: 1
allele frequency: 8.61341280642216e-6
allele num: 116098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3790C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1479C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1265C>T
  hgvsp: ENSP00000379475.1:p.Ser422Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.1031C>T
  hgvsp: ENSP00000392669.2:p.Ser344Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.556C>T
  hgvsp: ENSP00000406422.1:p.Ser186Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1310C>T
  hgvsp: ENSP00000412582.2:p.Ser437Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.112-35C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1265C>T
  hgvsp: ENSP00000416269.1:p.Ser422Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.737C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.*10C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser422Phe
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

6-31498617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498617
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498617
    reference: chr 6
allele count: 35
allele frequency: 2.997396546999178e-4
allele num: 116768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1232G>A
  hgvsp: ENSP00000365347.2:p.Cys411Tyr
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.975G>A
  hgvsp: ENST00000415382.2:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3734G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1209G>A
  hgvsp: ENST00000396172.1:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.500G>A
  hgvsp: ENST00000417023.1:c.500G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1209G>A
  hgvsp: ENST00000458640.1:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.96G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1254G>A
  hgvsp: ENST00000417556.2:c.1254G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.681G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1423G>A
  variant of: http://identifiers.org/hgnc/41999
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys411Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-31498633-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498633
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498633
    reference: chr 6
allele count: 1
allele frequency: 8.540438978563499e-6
allele num: 117090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1193A>G
  hgvsp: ENSP00000416269.1:p.Lys398Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1216A>G
  hgvsp: ENSP00000365347.2:p.Arg406Gly
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.484A>G
  hgvsp: ENSP00000406422.1:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.80A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.665A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1407A>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1238A>G
  hgvsp: ENSP00000412582.2:p.Lys413Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.959A>G
  hgvsp: ENSP00000392669.2:p.Lys320Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1193A>G
  hgvsp: ENSP00000379475.1:p.Lys398Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3718A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*124A>G
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8841
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys398Arg
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-31498650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498650
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498650
    reference: chr 6
allele count: 3
allele frequency: 2.552626652825758e-5
allele num: 117526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1176C>T
  hgvsp: ENST00000458640.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.648C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3701C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1199C>T
  hgvsp: ENSP00000365347.2:p.Pro400Leu
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*107C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1176C>T
  hgvsp: ENST00000396172.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.467C>T
  hgvsp: ENST00000417023.1:c.467C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1390C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.63C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.942C>T
  hgvsp: ENST00000415382.2:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1221C>T
  hgvsp: ENST00000417556.2:c.1221C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro400Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

6-31498659-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498659
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498659
    reference: chr 6
allele count: 1
allele frequency: 8.489108473828079e-6
allele num: 117798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1212A>G
  hgvsp: ENST00000417556.2:c.1212A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.639A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*98A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3692A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.54A>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1190A>G
  hgvsp: ENSP00000365347.2:p.His397Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.933A>G
  hgvsp: ENST00000415382.2:c.933A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.458A>G
  hgvsp: ENST00000417023.1:c.458A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1167A>G
  hgvsp: ENST00000458640.1:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1167A>G
  hgvsp: ENST00000396172.1:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1381A>G
  variant of: http://identifiers.org/hgnc/41999
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His397Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-31498677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498677
    reference: chr 6
allele count: 1
allele frequency: 8.458376330079678e-6
allele num: 118226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.36C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1172C>T
  hgvsp: ENSP00000365347.2:p.Pro391Leu
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.915C>T
  hgvsp: ENST00000415382.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1149C>T
  hgvsp: ENST00000396172.1:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1194C>T
  hgvsp: ENST00000417556.2:c.1194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1149C>T
  hgvsp: ENST00000458640.1:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.440C>T
  hgvsp: ENST00000417023.1:c.440C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1363C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.621C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3674C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*80C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro391Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-31498677-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498677
    reference: chr 6
allele count: 1
allele frequency: 8.458376330079678e-6
allele num: 118226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.440C>G
  hgvsp: ENST00000417023.1:c.440C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.915C>G
  hgvsp: ENST00000415382.2:c.915C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.36C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1172C>G
  hgvsp: ENSP00000365347.2:p.Pro391Arg
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1363C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1149C>G
  hgvsp: ENST00000396172.1:c.1149C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1194C>G
  hgvsp: ENST00000417556.2:c.1194C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1149C>G
  hgvsp: ENST00000458640.1:c.1149C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3674C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*80C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.621C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro391Arg
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-31498689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498689
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498689
    reference: chr 6
allele count: 1
allele frequency: 8.438391305081599e-6
allele num: 118506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.609C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.428C>T
  hgvsp: ENST00000417023.1:c.428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.903C>T
  hgvsp: ENST00000415382.2:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.24C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1182C>T
  hgvsp: ENST00000417556.2:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*68C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1137C>T
  hgvsp: ENST00000396172.1:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1351C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1160C>T
  hgvsp: ENSP00000365347.2:p.Ala387Val
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1137C>T
  hgvsp: ENST00000458640.1:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3662C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala387Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-31498707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498707
    reference: chr 6
allele count: 1
allele frequency: 8.40039649871474e-6
allele num: 119042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-4C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.6C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-4C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1142C>T
  hgvsp: ENSP00000365347.2:p.Ser381Phe
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-4C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser381Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-31498707-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498707
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498707
    reference: chr 6
allele count: 10
allele frequency: 8.400396498714739e-5
allele num: 119042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-4C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1142C>G
  hgvsp: ENSP00000365347.2:p.Ser381Cys
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-4C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.6C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser381Cys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

6-31498710-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498710
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498710
    reference: chr 6
allele count: 1
allele frequency: 8.386166180269028e-6
allele num: 119244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462421
  gene symbol: DDX39B
  hgvsc: ENST00000462421.1:n.3C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-7C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1139C>T
  hgvsp: ENSP00000365347.2:p.Pro380Leu
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-7C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-7C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro380Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

6-31498719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498719
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498719
    reference: chr 6
allele count: 1
allele frequency: 8.339727124128499e-6
allele num: 119908
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1130C>T
  hgvsp: ENSP00000365347.2:p.Pro377Leu
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-16C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-16C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-16C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3594
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro377Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

6-31498721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498721
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498721
    reference: chr 6
allele count: 4
allele frequency: 3.332777870354941e-5
allele num: 120020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-18C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1128C>T
  hgvsp: ENST00000376177.2:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-18C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-18C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr376Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-31498728-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498728
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498727
    reference: chr 6
allele count: 2
allele frequency: 1.662786830728301e-5
allele num: 120280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-3delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-26delC
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-26delC
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-26delC
  variant of: http://identifiers.org/hgnc/13917
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27843
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1123-3delC
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: TG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

6-31498736-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498736
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498736
    reference: chr 6
allele count: 5
allele frequency: 4.152685957277167e-5
allele num: 120404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-10G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-33G>C
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-33G>C
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-33G>C
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4449
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-31498736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498736
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498736
    reference: chr 6
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-33G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-10G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-33G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3598
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

6-31498737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498737
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498737
    reference: chr 6
allele count: 21978
allele frequency: 1.822055678068677e-1
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-34C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-11C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-34C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-34C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 2.25e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 5.75e1
  variant carriers: 2140
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 6.75e1
  variant carriers: 1126
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 3.25e1
  variant carriers: 1303
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 4.25e1
  variant carriers: 2492
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 519
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 8.75e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 5.25e1
  variant carriers: 2559
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 3.75e1
  variant carriers: 2023
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.75e1
  variant carriers: 755
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 6.25e1
  variant carriers: 1513
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 2731
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 7.25e1
  variant carriers: 759
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.75e1
  variant carriers: 506
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.25e1
  variant carriers: 344
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 8.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 9.25e1
  variant carriers: 66
num of homozygotes: 2104
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

6-31498743-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498743
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498742
    reference: chr 6
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-18delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-41delT
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-41delT
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-41delT
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: GA
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

6-31498752-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498752
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498752
    reference: chr 6
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-26G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-49G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-49G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-49G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3830
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

6-31498757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498757
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498757
    reference: chr 6
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-54C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-31C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-54C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-54C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

6-31498759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498759
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498759
    reference: chr 6
allele count: 12
allele frequency: 9.921783275180659e-5
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-56G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-33G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-56G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-56G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9180
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

6-31498761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498761
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498761
    reference: chr 6
allele count: 3
allele frequency: 2.479953707530793e-5
allele num: 120970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1123-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1123-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*54-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3648-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.595-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1123-35C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1337-58C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.414-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.889-58C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1168-58C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

6-31498786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498786
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498786
    reference: chr 6
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+44G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+44G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+44G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

6-31498789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498789
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498789
    reference: chr 6
allele count: 3
allele frequency: 2.476841531678803e-5
allele num: 121122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+41C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+41C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+41C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

6-31498789-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498789
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498789
    reference: chr 6
allele count: 6
allele frequency: 4.953683063357606e-5
allele num: 121122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+41C>G
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+41C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+41C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17927
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20212
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10679
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

6-31498806-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498806
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498807
    reference: chr 6
allele count: 2
allele frequency: 1.651664051531918e-5
allele num: 121090
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+23dupA
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+23dupA
  variant of: http://identifiers.org/hgnc/41999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-31498815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498815
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498815
    reference: chr 6
allele count: 3
allele frequency: 2.477046040029064e-5
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+15C>T
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+15C>T
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+15C>T
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

6-31498816-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498816
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498816
    reference: chr 6
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000365347
  ensembl transcript: ENST00000376177
  gene symbol: DDX39B
  hgvsc: ENST00000376177.2:c.1122+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000406422
  ensembl transcript: ENST00000417023
  gene symbol: DDX39B
  hgvsc: ENST00000417023.1:c.413+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000379475
  ensembl transcript: ENST00000396172
  gene symbol: DDX39B
  hgvsc: ENST00000396172.1:c.1122+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000474961
  gene symbol: DDX39B
  hgvsc: ENST00000474961.1:n.594+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254870
  ensembl protein: ENSP00000365356
  ensembl transcript: ENST00000376185
  gene symbol: ATP6V1G2-DDX39B
  hgvsc: ENST00000376185.1:c.*1336+14G>A
  variant of: http://identifiers.org/hgnc/41999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000416269
  ensembl transcript: ENST00000458640
  gene symbol: DDX39B
  hgvsc: ENST00000458640.1:c.1122+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000436220
  ensembl transcript: ENST00000484566
  gene symbol: DDX39B
  hgvsc: ENST00000484566.1:c.*53+14G>A
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000412582
  ensembl transcript: ENST00000417556
  gene symbol: DDX39B
  hgvsc: ENST00000417556.2:c.1167+14G>A
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10572
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

10-11911462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911462
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911462
    reference: chr 10
allele count: 5
allele frequency: 4.221689351210781e-5
allele num: 118436
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-27C>T
  variant of: http://identifiers.org/hgnc/23728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.167G>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.665G>A
  variant of: http://identifiers.org/hgnc/27343
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22482
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8078
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41171
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-11911464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911464
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911464
    reference: chr 10
allele count: 11
allele frequency: 9.278941863211526e-5
allele num: 118548
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-25C>T
  variant of: http://identifiers.org/hgnc/23728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.165G>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.663G>A
  variant of: http://identifiers.org/hgnc/27343
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25054
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22627
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41645
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

10-11911465-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911465
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911465
    reference: chr 10
allele count: 2
allele frequency: 1.68625533278249e-5
allele num: 118606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.164T>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.662T>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-24A>T
  variant of: http://identifiers.org/hgnc/23728
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-11911475-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911475
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911475
    reference: chr 10
allele count: 2
allele frequency: 1.68214237653075e-5
allele num: 118896
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.652G>T
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.154G>T
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-14C>A
  variant of: http://identifiers.org/hgnc/23728
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23332
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42820
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 2
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

10-11911476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911476
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911476
    reference: chr 10
allele count: 1
allele frequency: 8.407883231317684e-6
allele num: 118936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.153G>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.651G>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-13C>T
  variant of: http://identifiers.org/hgnc/23728
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25635
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

10-11911477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911477
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911477
    reference: chr 10
allele count: 1
allele frequency: 8.406610958858046e-6
allele num: 118954
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-12C>T
  variant of: http://identifiers.org/hgnc/23728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.152G>A
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.650G>A
  variant of: http://identifiers.org/hgnc/27343
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

10-11911480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911480
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911480
    reference: chr 10
allele count: 1
allele frequency: 8.398562166157153e-6
allele num: 119068
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.647C>T
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.149C>T
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-9G>A
  variant of: http://identifiers.org/hgnc/23728
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43526
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

10-11911481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11911481
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 11911481
    reference: chr 10
allele count: 1
allele frequency: 8.394754957102802e-6
allele num: 119122
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148426
  ensembl protein: ENSP00000277570
  ensembl transcript: ENST00000277570
  gene symbol: PROSER2
  hgvsc: ENST00000277570.5:c.392-8T>C
  variant of: http://identifiers.org/hgnc/23728
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000445498
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000445498.1:n.646A>G
  variant of: http://identifiers.org/hgnc/27343
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000225778
  ensembl transcript: ENST00000453242
  gene symbol: PROSER2-AS1
  hgvsc: ENST00000453242.1:n.148A>G
  variant of: http://identifiers.org/hgnc/27343
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8383
  bin: 6.75e1
  variant carriers: 0
hgvs: c.392-8T>C
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-31498819-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31498819
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31498819
    reference: chr 6
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl protein: ENSP00000392669
  ensembl transcript: ENST00000415382
  gene symbol: DDX39B
  hgvsc: ENST00000415382.2:c.888+11C>G
  variant of: http://identifiers.org/hgnc/13917
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198563
  ensembl transcript: ENST00000462256
  gene symbol: DDX39B
  hgvsc: ENST00000462256.1:n.3647+11C>G
  variant of: http://identifiers.org/hgnc/13917
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 4207
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29198
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 9149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.207324643078833e-5
allele num: 16110
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.990562740300594e-4
allele num: 11444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.499081755430309e-5
allele num: 63164
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.177e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.379e0

FS
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 2.375254e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 2332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29192
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.199628022318661e-5
allele num: 16130
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.166460846711631e-5
allele num: 63162
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 6.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

DP
type: SiteQuality
SIO_000300: 2.37658e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9492
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4276
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29199
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582428711586543e-5
allele num: 63194
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.107e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 2.379825e6

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29204
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3289
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 7.25e1
variant carriers: 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: 16180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.746419839329375e-3
allele num: 11452
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.069e1

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.412e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

DP
type: SiteQuality
SIO_000300: 2.382806e6

GenotypeQuality
all individuals: 3518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29200
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63222
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.709e-1

FS
type: SiteQuality
SIO_000300: 6.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

DP
type: SiteQuality
SIO_000300: 2.382902e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 7.45e0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29200
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63222
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.092896174863388e-4
allele num: 9150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 2.382902e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 7.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.709e-1

FS
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

GenotypeQuality
all individuals: 2304
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4184
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3423
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 450
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 251
allele frequency: 2.741371778069026e-2
allele num: 9156
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 14
allele frequency: 2.118003025718608e-3
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 160
allele frequency: 9.877762686751451e-3
allele num: 16198
num of homozygotes: 2

Latino
type: Population
allele count: 129
allele frequency: 1.126244106862232e-2
allele num: 11454
num of homozygotes: 1

Other
type: Population
allele count: 10
allele frequency: 1.152073732718894e-2
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.523608174770966e-4
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 913
allele frequency: 1.443980514961726e-2
allele num: 63228
num of homozygotes: 13

QD
type: SiteQuality
SIO_000300: 1.088e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.175e0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

DP
type: SiteQuality
SIO_000300: 2.419849e6

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 3197
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30017
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.173601679219657e-5
allele num: 16198
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.82961992136304e-4
allele num: 9156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63228
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 2.419849e6

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

FS
type: SiteQuality
SIO_000300: 1.175e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

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

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3503
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9539
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
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GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3282
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variant carriers: 0

GenotypeQuality
all individuals: 2365
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variant carriers: 0

GenotypeQuality
all individuals: 29251
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4335
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63246
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.169792694965449e-5
allele num: 16208
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.49e-2

FS
type: SiteQuality
SIO_000300: 3.29e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.791e1

DP
type: SiteQuality
SIO_000300: 2.401513e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.254e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4332
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 169
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 2354
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GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 524
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GenotypeQuality
all individuals: 9501
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 3506
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GenotypeQuality
all individuals: 3286
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 29247
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580877703300873e-5
allele num: 63256
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 2.402288e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.285e0

QD
type: SiteQuality
SIO_000300: 1.147e1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

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

GenotypeQuality
all individuals: 294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.5e0
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GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
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GenotypeQuality
all individuals: 3383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3495
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29243
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4076
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.182762458266353e-5
allele num: 16174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.936e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

FS
type: SiteQuality
SIO_000300: 7.849e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

QD
type: SiteQuality
SIO_000300: 1.048e1

DP
type: SiteQuality
SIO_000300: 2.421127e6

GenotypeQuality
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29243
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 379
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3495
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59846547314578e-5
allele num: 62560
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.427715e6

MQ
type: SiteQuality
SIO_000300: 5.905e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

FS
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: 7.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.072e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 7.23e0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 453
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 2778
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2919
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variant carriers: 5

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 150
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 86
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variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2758
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1980
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variant carriers: 7

GenotypeQuality
all individuals: 6924
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1812
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 35079
bin: 9.75e1
variant carriers: 9125

GenotypeQuality
all individuals: 3316
bin: 6.75e1
variant carriers: 3

Other
type: Population
allele count: 44
allele frequency: 5.057471264367816e-2
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 482
allele frequency: 7.291981845688351e-2
allele num: 6610
num of homozygotes: 11

South Asian
type: Population
allele count: 647
allele frequency: 3.993827160493827e-2
allele num: 16200
num of homozygotes: 19

Latino
type: Population
allele count: 348
allele frequency: 3.037709497206704e-2
allele num: 11456
num of homozygotes: 8

European (Non-Finnish)
type: Population
allele count: 6303
allele frequency: 9.966477973498625e-2
allele num: 63242
num of homozygotes: 345

African
type: Population
allele count: 1065
allele frequency: 1.163934426229508e-1
allele num: 9150
num of homozygotes: 60

East Asian
type: Population
allele count: 764
allele frequency: 8.979783732957217e-2
allele num: 8508
num of homozygotes: 28

BaseQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.491e1

DP
type: SiteQuality
SIO_000300: 2.633991e6

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
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variant carriers: 0

GenotypeQuality
all individuals: 7631
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 2247
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GenotypeQuality
all individuals: 3851
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GenotypeQuality
all individuals: 3275
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GenotypeQuality
all individuals: 2122
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 189
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GenotypeQuality
all individuals: 3408
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GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 31668
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581127660247289e-5
allele num: 63246
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.477991e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 2235
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GenotypeQuality
all individuals: 7402
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GenotypeQuality
all individuals: 31667
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 214
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GenotypeQuality
all individuals: 3406
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 2116
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GenotypeQuality
all individuals: 3793
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 3276
bin: 9.25e1
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GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63252
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.177415369409439e-5
allele num: 16188
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-1

QD
type: SiteQuality
SIO_000300: 6.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

DP
type: SiteQuality
SIO_000300: 2.476432e6

FS
type: SiteQuality
SIO_000300: 4.806e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

VQSLOD
type: SiteQuality
SIO_000300: -1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

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

GenotypeQuality
all individuals: 31665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 1.75e1
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GenotypeQuality
all individuals: 554
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variant carriers: 0

GenotypeQuality
all individuals: 222
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variant carriers: 0

GenotypeQuality
all individuals: 271
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GenotypeQuality
all individuals: 2114
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GenotypeQuality
all individuals: 3272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3198
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63240
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 1.418e1

VQSLOD
type: SiteQuality
SIO_000300: 7.65e-1

DP
type: SiteQuality
SIO_000300: 2.474148e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

FS
type: SiteQuality
SIO_000300: 3.854e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
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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bin: 9.75e1
variant carriers: 5

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.905138339920949e-5
allele num: 63250
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.43e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.735e0

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 2.472567e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.092418614813196e-4
allele num: 9154
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63238
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.762e0

DP
type: SiteQuality
SIO_000300: 2.471059e6

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.097e1

FS
type: SiteQuality
SIO_000300: 8.279e0

MQRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63226
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.092657342657343e-4
allele num: 9152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.705e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 1.655e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 2.469571e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

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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variant carriers: 4

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.355704697986577e-4
allele num: 8940
num of homozygotes: 0

European (Finnish)
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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: 15660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62948
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

FS
type: SiteQuality
SIO_000300: 3.661e0

MQ
type: SiteQuality
SIO_000300: 5.798e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.43e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.293642e6

VQSLOD
type: SiteQuality
SIO_000300: -1.646e0

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.393044367727913e-5
allele num: 15642
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62950
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.268e0

VQSLOD
type: SiteQuality
SIO_000300: -1.062e-1

InbreedingCoeff
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SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.935e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8942
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.845e1

MQRankSum
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FS
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QD
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8940
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62964
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

East Asian
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allele frequency: 1.176193836744295e-4
allele num: 8502
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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South Asian
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Latino
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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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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South Asian
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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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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Other
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East Asian
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African
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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DP
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ReadPosRankSum
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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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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele num: 63020
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South Asian
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Other
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FS
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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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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East Asian
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Latino
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Other
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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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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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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African
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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South Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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DP
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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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bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16004
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584384308257811e-5
allele num: 63116
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

FS
type: SiteQuality
SIO_000300: 3.647e0

DP
type: SiteQuality
SIO_000300: 2.33328e6

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.165258126800241e-5
allele num: 63186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9082
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.0512e1

DP
type: SiteQuality
SIO_000300: 2.342605e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

VQSLOD
type: SiteQuality
SIO_000300: -8.517e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.131e1

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3824
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9136
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.162188809465122e-5
allele num: 16228
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.071e0

FS
type: SiteQuality
SIO_000300: 6.604e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.161e0

DP
type: SiteQuality
SIO_000300: 2.34902e6

VQSLOD
type: SiteQuality
SIO_000300: -2.044e0

QD
type: SiteQuality
SIO_000300: 7.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.836e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.79e-1

GenotypeDepth
all individuals: 4215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 35

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

African
type: Population
allele count: 35
allele frequency: 3.761014399312272e-3
allele num: 9306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63572
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.361317e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.235e0

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

FS
type: SiteQuality
SIO_000300: 5.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

GenotypeDepth
all individuals: 1102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3836
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 3992
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 912
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.364287e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.099e1

FS
type: SiteQuality
SIO_000300: 4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

VQSLOD
type: SiteQuality
SIO_000300: -2.506e0

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e0

GenotypeDepth
all individuals: 524
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4002
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.121878121878122e-5
allele num: 64064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.379e1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 7.58e-1

DP
type: SiteQuality
SIO_000300: 2.369347e6

GenotypeDepth
all individuals: 2714
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 66
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GenotypeQuality
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GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 27817
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4383
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.057305984351871e-4
allele num: 9458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.372095e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
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SIO_000300: 5.39e-1

BaseQRankSum
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SIO_000300: 8.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 1.503e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 4014
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27816
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2460
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549186676994578e-5
allele num: 64550
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.376904e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 5.204e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

GenotypeDepth
all individuals: 8887
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3861
bin: 8.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64550
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 5.204e0

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 2.376904e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9698
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.042970379641218e-4
allele num: 9588
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64742
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 2.379627e6

QD
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.612e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

GenotypeDepth
all individuals: 1729
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1103
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variant carriers: 0

GenotypeQuality
all individuals: 27827
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65126
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.172e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 2.383669e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeDepth
all individuals: 8914
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 746
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 10

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.228388047784295e-4
allele num: 65126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 2.383669e6

GenotypeDepth
all individuals: 178
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variant carriers: 0

GenotypeDepth
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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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GenotypeQuality
all individuals: 2824
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65270
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 2.385639e6

MQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.25e-1

QD
type: SiteQuality
SIO_000300: 1.836e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-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
all individuals: 125
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
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Other
type: Population
allele count: 0
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East Asian
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.045e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 3.139e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

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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bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.996001599360256e-5
allele num: 10004
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.55913194127838e-5
allele num: 65802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
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DP
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FS
type: SiteQuality
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: 4.11e-1

ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4067
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031497256494983e-5
allele num: 65974
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 7.726e0

DP
type: SiteQuality
SIO_000300: 2.395127e6

QD
type: SiteQuality
SIO_000300: 1.407e1

MQ
type: SiteQuality
SIO_000300: 6.007e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
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GenotypeQuality
all individuals: 568
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27852
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.326007959854646e-4
allele num: 11558
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.46e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

DP
type: SiteQuality
SIO_000300: 2.396827e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 1.838e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

GenotypeQuality
all individuals: 214
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
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GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
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GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27852
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2483
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 1.838e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
type: SiteQuality
SIO_000300: 2.396827e6

GenotypeQuality
all individuals: 3163
bin: 6.75e1
variant carriers: 29

GenotypeQuality
all individuals: 1765
bin: 8.75e1
variant carriers: 40

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 10

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 6745
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 12

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 21

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 145
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 401
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 37090
bin: 9.75e1
variant carriers: 19499

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2950
bin: 7.75e1
variant carriers: 49

GenotypeQuality
all individuals: 2075
bin: 7.25e1
variant carriers: 24

South Asian
type: Population
allele count: 4143
allele frequency: 2.511517943743938e-1
allele num: 16496
num of homozygotes: 566

Latino
type: Population
allele count: 1508
allele frequency: 1.306080027715226e-1
allele num: 11546
num of homozygotes: 117

African
type: Population
allele count: 1515
allele frequency: 1.487043580683157e-1
allele num: 10188
num of homozygotes: 98

European (Non-Finnish)
type: Population
allele count: 11964
allele frequency: 1.805777764361397e-1
allele num: 66254
num of homozygotes: 1080

East Asian
type: Population
allele count: 1433
allele frequency: 1.660871580899397e-1
allele num: 8628
num of homozygotes: 111

European (Finnish)
type: Population
allele count: 1239
allele frequency: 1.875567665758401e-1
allele num: 6606
num of homozygotes: 117

Other
type: Population
allele count: 176
allele frequency: 1.946902654867257e-1
allele num: 904
num of homozygotes: 15

BaseQRankSum
type: SiteQuality
SIO_000300: -1.312e0

DP
type: SiteQuality
SIO_000300: 2.616434e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 1.61e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4493
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27976
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2939
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015408738654524e-5
allele num: 66326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 2.154e1

DP
type: SiteQuality
SIO_000300: 2.435121e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.311e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 2.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4035
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27959
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 2.433564e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.37e0

QD
type: SiteQuality
SIO_000300: 3.478e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.25e1
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GenotypeQuality
all individuals: 8238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2672
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27969
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4047
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.336e1

DP
type: SiteQuality
SIO_000300: 2.432271e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 1.145e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.194e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.69e-1

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.75e1
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GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8140
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3830
bin: 9.25e1
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GenotypeQuality
all individuals: 4335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.25e1
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GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
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GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
all individuals: 27976
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2937
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2672
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 12
allele frequency: 1.170046801872075e-3
allele num: 10256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.804e0

QD
type: SiteQuality
SIO_000300: 1.152e1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 2.432296e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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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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allele frequency: 9.738994935722633e-5
allele num: 10268
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Latino
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allele frequency: 8.647526807333103e-5
allele num: 11564
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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FS
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MQRankSum
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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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European (Non-Finnish)
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allele frequency: 1.50195253829979e-5
allele num: 66580
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East Asian
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Latino
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allele frequency: 0.0e0
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South Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.506534474988734e-5
allele num: 66570
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Latino
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Other
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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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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allele frequency: 3.639451655950503e-4
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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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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South 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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Other
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East Asian
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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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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: 3.00507858280494e-5
allele num: 66554
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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DP
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BaseQRankSum
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QD
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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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African
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East Asian
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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VQSLOD
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.192e0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
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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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65114
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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MQRankSum
type: SiteQuality
SIO_000300: -5.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.65e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 6.743e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

DP
type: SiteQuality
SIO_000300: 1.491571e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6440
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South Asian
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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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European (Non-Finnish)
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allele count: 2
allele frequency: 3.066732090284593e-5
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num of homozygotes: 0

African
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Other
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Latino
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 3.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.506984e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.44e-1

QD
type: SiteQuality
SIO_000300: 1.161e1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele num: 876
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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Latino
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.508577e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

GenotypeQuality
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variant carriers: 1

South Asian
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allele count: 0
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Other
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allele count: 0
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East Asian
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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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10092
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.532895947023116e-5
allele num: 65236
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.510397e6

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

QD
type: SiteQuality
SIO_000300: 3.126e1

VQSLOD
type: SiteQuality
SIO_000300: -3.251e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 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 count: 1
allele frequency: 1.531721961829489e-5
allele num: 65286
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Other
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Latino
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.652e0

FS
type: SiteQuality
SIO_000300: 8.109999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 1.513582e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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Other
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Latino
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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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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.514911e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.51e-1

QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.21e-1

ReadPosRankSum
type: SiteQuality
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