22-18189613-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189613
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189612
    reference: chr 22
allele count: 1
allele frequency: 8.866820358219543e-6
allele num: 112780
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17706delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+23delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4462delT
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17706delT
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: CT
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

22-18189613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189613
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189613
    reference: chr 22
allele count: 1
allele frequency: 8.866820358219543e-6
allele num: 112780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+22C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4461C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17705C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4461C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4461C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4461C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4461C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17705C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4461C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-18189615-CCGTCGTCACATGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189615
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189601
    reference: chr 22
allele count: 1
allele frequency: 8.866820358219543e-6
allele num: 112780
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: CCGTCGTCACATGAT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

22-18189616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189616
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189616
    reference: chr 22
allele count: 6
allele frequency: 5.320186561208746e-5
allele num: 112778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17708C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+25C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4464C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4464C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4464C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17708C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4464C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4464C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4464C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

22-18189617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189617
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189617
    reference: chr 22
allele count: 96
allele frequency: 8.511996595201362e-4
allele num: 112782
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4465G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4465G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+26G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4465G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17709G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4465G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17709G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4465G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4465G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 9.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-18189619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189619
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189619
    reference: chr 22
allele count: 1
allele frequency: 8.866820358219543e-6
allele num: 112780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4467C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4467C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4467C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4467C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4467C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17711C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+28C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17711C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4467C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

22-18189620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189620
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189620
    reference: chr 22
allele count: 14
allele frequency: 1.241332836800199e-4
allele num: 112782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+29G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17712G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4468G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17712G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

22-18189620-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189620
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189620
    reference: chr 22
allele count: 2
allele frequency: 1.773332624000284e-5
allele num: 112782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4468G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4468G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17712G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17712G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4468G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4468G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+29G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4468G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4468G>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51868
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

22-18189628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189628
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189628
    reference: chr 22
allele count: 1
allele frequency: 8.866820358219543e-6
allele num: 112780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17720A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17720A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4476A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+37A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51868
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-18189631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189631
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189631
    reference: chr 22
allele count: 1
allele frequency: 8.86713485138682e-6
allele num: 112776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+40A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17723A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4479A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17723A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/22-18189638-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189638
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189638
    reference: chr 22
allele count: 2
allele frequency: 1.773489873372823e-5
allele num: 112772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17730C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17730C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4486C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+47C>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51866
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

22-18189641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18189641
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18189641
    reference: chr 22
allele count: 7
allele frequency: 6.207104474435596e-5
allele num: 112774
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.600+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*206+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.386+17733G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*169+17733G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*98+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.114+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.114+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.228+4489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.116+50G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51865
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

22-18209399-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209399
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209399
    reference: chr 22
allele count: 1
allele frequency: 8.728288382648164e-6
allele num: 114570
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-44A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-44A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19765
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

22-18209406-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209406
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209406
    reference: chr 22
allele count: 1
allele frequency: 8.719155985700584e-6
allele num: 114690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-37C>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-37C>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19790
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

22-18209415-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209415
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209415
    reference: chr 22
allele count: 4
allele frequency: 3.471559250837514e-5
allele num: 115222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-28A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-28A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8800
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

22-18209419-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209419
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209419
    reference: chr 22
allele count: 1
allele frequency: 8.646031471554556e-6
allele num: 115660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-24T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-24T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8805
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3149
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-18209423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209423
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209423
    reference: chr 22
allele count: 8
allele frequency: 6.892748828232699e-5
allele num: 116064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-20C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-20C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4307
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4944
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-18209425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209425
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209425
    reference: chr 22
allele count: 2
allele frequency: 1.712211492363537e-5
allele num: 116808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-18C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-18C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4314
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4979
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

22-18209426-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209426
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209426
    reference: chr 22
allele count: 1
allele frequency: 8.540001366400219e-6
allele num: 117096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-17T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-17T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

22-18209427-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209427
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209427
    reference: chr 22
allele count: 5
allele frequency: 4.262501918125863e-5
allele num: 117302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.387-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.115-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.115-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*207-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*99-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.229-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.601-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.117-16T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*170-16T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-18209447-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209447
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209447
    reference: chr 22
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.119C>A
  hgvsp: ENSP00000338932.5:p.Thr40Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.391C>A
  hgvsp: ENSP00000347133.3:p.Leu131Met
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.605C>A
  hgvsp: ENSP00000318883.5:p.Thr202Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*103C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*211C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.119C>A
  hgvsp: ENSP00000437667.1:p.Thr40Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.233C>A
  hgvsp: ENSP00000441344.1:p.Thr78Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*174C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.121C>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13034
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr202Asn
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

22-18209451-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209451
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209451
    reference: chr 22
allele count: 1
allele frequency: 8.299030673217368e-6
allele num: 120496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.395G>A
  hgvsp: ENSP00000347133.3:p.Cys132Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.123G>A
  hgvsp: ENST00000337612.5:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.123G>A
  hgvsp: ENST00000543133.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.125G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.237G>A
  hgvsp: ENST00000538149.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.609G>A
  hgvsp: ENST00000317582.5:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*178G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*215G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys132Tyr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-18209457-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209457
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209457
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*184T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.615T>A
  hgvsp: ENSP00000318883.5:p.Ser205Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.243T>A
  hgvsp: ENSP00000441344.1:p.Ser81Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*221T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*113T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.129T>A
  hgvsp: ENSP00000338932.5:p.Ser43Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.401T>A
  hgvsp: ENSP00000347133.3:p.Val134Asp
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.129T>A
  hgvsp: ENSP00000437667.1:p.Ser43Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.131T>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11823
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser205Arg
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-18209457-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209457
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209457
    reference: chr 22
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.243T>C
  hgvsp: ENST00000538149.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.129T>C
  hgvsp: ENST00000543133.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*113T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*184T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*221T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.131T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.401T>C
  hgvsp: ENSP00000347133.3:p.Val134Ala
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.615T>C
  hgvsp: ENST00000317582.5:c.615T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.129T>C
  hgvsp: ENST00000337612.5:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5222
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6022
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val134Ala
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

22-18209459-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209459
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209459
    reference: chr 22
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.133T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.131T>A
  hgvsp: ENSP00000437667.1:p.Leu44His
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*115T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*186T>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.245T>A
  hgvsp: ENSP00000441344.1:p.Leu82His
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.617T>A
  hgvsp: ENSP00000318883.5:p.Leu206His
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.403T>A
  hgvsp: ENSP00000347133.3:p.Leu135Met
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.131T>A
  hgvsp: ENSP00000338932.5:p.Leu44His
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*223T>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19866
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu206His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-18209471-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209471
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209471
    reference: chr 22
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.629A>G
  hgvsp: ENSP00000318883.5:p.Glu210Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*127A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.143A>G
  hgvsp: ENSP00000338932.5:p.Glu48Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.143A>G
  hgvsp: ENSP00000437667.1:p.Glu48Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.145A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*235A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*198A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.415A>G
  hgvsp: ENSP00000347133.3:p.Arg139Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.257A>G
  hgvsp: ENSP00000441344.1:p.Glu86Gly
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu210Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

22-18209475-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209475
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209475
    reference: chr 22
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*202G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.147G>A
  hgvsp: ENST00000543133.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*239G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.419G>A
  hgvsp: ENSP00000347133.3:p.Arg140Lys
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.261G>A
  hgvsp: ENST00000538149.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.149G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.147G>A
  hgvsp: ENST00000337612.5:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.633G>A
  hgvsp: ENST00000317582.5:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*131G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13256
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19884
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg140Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

22-18209481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209481
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209481
    reference: chr 22
allele count: 2
allele frequency: 1.649348507339601e-5
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.153C>T
  hgvsp: ENST00000543133.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.425C>T
  hgvsp: ENSP00000347133.3:p.Thr142Ile
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*137C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.153C>T
  hgvsp: ENST00000337612.5:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.155C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.639C>T
  hgvsp: ENST00000317582.5:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*208C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*245C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.267C>T
  hgvsp: ENST00000538149.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5305
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr142Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

22-18209496-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209496
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209496
    reference: chr 22
allele count: 268
allele frequency: 2.208451447030127e-3
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*152A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.282A>G
  hgvsp: ENST00000538149.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.170A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.168A>G
  hgvsp: ENST00000543133.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*260A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.168A>G
  hgvsp: ENST00000337612.5:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.654A>G
  hgvsp: ENST00000317582.5:c.654A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.440A>G
  hgvsp: ENSP00000347133.3:p.Gln147Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*223A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 8897
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 11978
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11894
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 5.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln147Arg
num of homozygotes: 3
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

22-18209500-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209500
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209500
    reference: chr 22
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.172G>T
  hgvsp: ENSP00000437667.1:p.Asp58Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*227G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.444G>T
  hgvsp: ENSP00000347133.3:p.Lys148Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.174G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.286G>T
  hgvsp: ENSP00000441344.1:p.Asp96Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.658G>T
  hgvsp: ENSP00000318883.5:p.Asp220Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.172G>T
  hgvsp: ENSP00000338932.5:p.Asp58Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*156G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*264G>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp220Tyr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

22-18209502-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209502
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209502
    reference: chr 22
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.446T>C
  hgvsp: ENSP00000347133.3:p.Ile149Thr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*266T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.176T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.174T>C
  hgvsp: ENST00000337612.5:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.288T>C
  hgvsp: ENST00000538149.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.174T>C
  hgvsp: ENST00000543133.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*158T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.660T>C
  hgvsp: ENST00000317582.5:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*229T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile149Thr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

22-18209507-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209507
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209507
    reference: chr 22
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.451A>G
  hgvsp: ENSP00000347133.3:p.Met151Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.665A>G
  hgvsp: ENSP00000318883.5:p.Asn222Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*271A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*234A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.179A>G
  hgvsp: ENSP00000437667.1:p.Asn60Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*163A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.179A>G
  hgvsp: ENSP00000338932.5:p.Asn60Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.293A>G
  hgvsp: ENSP00000441344.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.181A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn222Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-18209517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209517
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209517
    reference: chr 22
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.189C>T
  hgvsp: ENST00000337612.5:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.189C>T
  hgvsp: ENST00000543133.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.675C>T
  hgvsp: ENST00000317582.5:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.461C>T
  hgvsp: ENSP00000347133.3:p.Thr154Ile
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.303C>T
  hgvsp: ENST00000538149.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*244C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.191C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr154Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/22-18209518-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209518
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209518
    reference: chr 22
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.462A>C
  hgvsp: ENST00000355028.3:c.462A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.190A>C
  hgvsp: ENSP00000437667.1:p.Ile64Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*245A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*282A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.190A>C
  hgvsp: ENSP00000338932.5:p.Ile64Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.192A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.304A>C
  hgvsp: ENSP00000441344.1:p.Ile102Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*174A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.676A>C
  hgvsp: ENSP00000318883.5:p.Ile226Leu
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile226Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

22-18209518-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209518
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209518
    reference: chr 22
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.462A>G
  hgvsp: ENST00000355028.3:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.190A>G
  hgvsp: ENSP00000338932.5:p.Ile64Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.192A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.304A>G
  hgvsp: ENSP00000441344.1:p.Ile102Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.190A>G
  hgvsp: ENSP00000437667.1:p.Ile64Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*174A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.676A>G
  hgvsp: ENSP00000318883.5:p.Ile226Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*245A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*282A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6151
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19997
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile226Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-18209524-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209524
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209524
    reference: chr 22
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*180C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.196C>A
  hgvsp: ENSP00000437667.1:p.Pro66Thr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*288C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.310C>A
  hgvsp: ENSP00000441344.1:p.Pro104Thr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.198C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.468C>A
  hgvsp: ENSP00000347133.3:p.Cys156Ter
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.682C>A
  hgvsp: ENSP00000318883.5:p.Pro228Thr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*251C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.196C>A
  hgvsp: ENSP00000338932.5:p.Pro66Thr
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys156Ter
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

22-18209524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209524
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209524
    reference: chr 22
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*180C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.468C>T
  hgvsp: ENST00000355028.3:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.682C>T
  hgvsp: ENSP00000318883.5:p.Pro228Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.198C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.310C>T
  hgvsp: ENSP00000441344.1:p.Pro104Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.196C>T
  hgvsp: ENSP00000338932.5:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.196C>T
  hgvsp: ENSP00000437667.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*288C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*251C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro228Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-18209529-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209529
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209529
    reference: chr 22
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.315C>A
  hgvsp: ENSP00000441344.1:p.Ser105Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.201C>A
  hgvsp: ENSP00000338932.5:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.473C>A
  hgvsp: ENSP00000347133.3:p.Ala158Glu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*185C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.203C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.687C>A
  hgvsp: ENSP00000318883.5:p.Ser229Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*293C>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.201C>A
  hgvsp: ENSP00000437667.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*256C>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12031
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20001
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser229Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

22-18209529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209529
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209529
    reference: chr 22
allele count: 5
allele frequency: 4.118548294097296e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*256C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.473C>T
  hgvsp: ENSP00000347133.3:p.Ala158Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.315C>T
  hgvsp: ENST00000538149.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*293C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*185C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.201C>T
  hgvsp: ENST00000337612.5:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.687C>T
  hgvsp: ENST00000317582.5:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.203C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.201C>T
  hgvsp: ENST00000543133.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13229
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala158Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

22-18209530-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209530
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209530
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*294G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*257G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.204G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.688G>A
  hgvsp: ENSP00000318883.5:p.Asp230Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.474G>A
  hgvsp: ENST00000355028.3:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.202G>A
  hgvsp: ENSP00000338932.5:p.Asp68Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.316G>A
  hgvsp: ENSP00000441344.1:p.Asp106Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.202G>A
  hgvsp: ENSP00000437667.1:p.Asp68Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*186G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20001
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp230Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

22-18209530-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209530
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209530
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.316G>T
  hgvsp: ENSP00000441344.1:p.Asp106Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*294G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.688G>T
  hgvsp: ENSP00000318883.5:p.Asp230Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.202G>T
  hgvsp: ENSP00000437667.1:p.Asp68Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*257G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.474G>T
  hgvsp: ENST00000355028.3:c.474G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*186G>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.202G>T
  hgvsp: ENSP00000338932.5:p.Asp68Tyr
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.204G>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp230Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/22-18209541-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209541
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209540
    reference: chr 22
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.486delC
  hgvsp: ENSP00000347133.3:p.Asp162GlufsTer17
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.216delC
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.214delC
  hgvsp: ENSP00000338932.5:p.Gln72LysfsTer10
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.214delC
  hgvsp: ENSP00000437667.1:p.Gln72LysfsTer10
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*306delC
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.700delC
  hgvsp: ENSP00000318883.5:p.Gln234LysfsTer10
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.328delC
  hgvsp: ENSP00000441344.1:p.Gln110LysfsTer10
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*269delC
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*198delC
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln234LysfsTer10
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: AC
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

22-18209555-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209555
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209553
    reference: chr 22
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.344_345delAG
  hgvsp: ENSP00000441344.1:p.Glu115ValfsTer11
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.502_503delAG
  hgvsp: ENSP00000347133.3:p.Leu169ProfsTer246
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*285_*286delAG
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*322_*323delAG
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.230_231delAG
  hgvsp: ENSP00000338932.5:p.Glu77ValfsTer11
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.232_233delAG
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.230_231delAG
  hgvsp: ENSP00000437667.1:p.Glu77ValfsTer11
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.716_717delAG
  hgvsp: ENSP00000318883.5:p.Glu239ValfsTer11
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*214_*215delAG
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20003
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu239ValfsTer11
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: CAG
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-18209556-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209556
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209556
    reference: chr 22
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.500A>G
  hgvsp: ENSP00000347133.3:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.228A>G
  hgvsp: ENST00000543133.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*283A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.342A>G
  hgvsp: ENST00000538149.1:c.342A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.714A>G
  hgvsp: ENST00000317582.5:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*212A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*320A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.228A>G
  hgvsp: ENST00000337612.5:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.230A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln167Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

22-18209592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209592
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209592
    reference: chr 22
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*248G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.266G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*319G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.750G>A
  hgvsp: ENST00000317582.5:c.750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*20G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*356G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.264G>A
  hgvsp: ENST00000337612.5:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.264G>A
  hgvsp: ENST00000543133.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.378G>A
  hgvsp: ENST00000538149.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu250Glu
num of homozygotes: 1
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

22-18209599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209599
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209599
    reference: chr 22
allele count: 38
allele frequency: 3.130354553842098e-4
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.385C>T
  hgvsp: ENSP00000441344.1:p.Pro129Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.757C>T
  hgvsp: ENSP00000318883.5:p.Pro253Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*255C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.271C>T
  hgvsp: ENSP00000338932.5:p.Pro91Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*363C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.271C>T
  hgvsp: ENSP00000437667.1:p.Pro91Ser
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*326C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*27C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.273C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro253Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

22-18209609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209609
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209609
    reference: chr 22
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.395T>C
  hgvsp: ENSP00000441344.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.767T>C
  hgvsp: ENSP00000318883.5:p.Leu256Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*336T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.283T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*373T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*265T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.281T>C
  hgvsp: ENSP00000338932.5:p.Leu94Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*37T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.281T>C
  hgvsp: ENSP00000437667.1:p.Leu94Pro
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4414
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu256Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

22-18209612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209612
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209612
    reference: chr 22
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.770C>T
  hgvsp: ENSP00000318883.5:p.Ser257Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.284C>T
  hgvsp: ENSP00000437667.1:p.Ser95Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.398C>T
  hgvsp: ENSP00000441344.1:p.Ser133Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.286C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*40C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.284C>T
  hgvsp: ENSP00000338932.5:p.Ser95Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*376C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*268C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*339C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser257Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-18209613-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209613
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209613
    reference: chr 22
allele count: 71680
allele frequency: 5.913605913605914e-1
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.285A>G
  hgvsp: ENST00000543133.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.287A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*269A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*377A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.399A>G
  hgvsp: ENST00000538149.1:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*41A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.771A>G
  hgvsp: ENST00000317582.5:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*340A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.285A>G
  hgvsp: ENST00000337612.5:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 4.75e1
  variant carriers: 5938
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 2.25e1
  variant carriers: 532
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 7.25e1
  variant carriers: 2282
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 5684
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 2.75e1
  variant carriers: 1207
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 8.75e1
  variant carriers: 936
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 4.25e1
  variant carriers: 5043
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 6.25e1
  variant carriers: 4556
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 3.75e1
  variant carriers: 3637
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 790
genotype depth: GenotypeDepth
  all individuals: 6425
  bin: 5.25e1
  variant carriers: 6136
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 9.75e1
  variant carriers: 4493
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 1592
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 8.25e1
  variant carriers: 1136
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.25e1
  variant carriers: 2196
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 6.75e1
  variant carriers: 3314
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 224
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 8.25e1
  variant carriers: 283
hgvs: p.Ser257Ser
num of homozygotes: 22008
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/22-18209617-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209617
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209617
    reference: chr 22
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*344A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.403A>C
  hgvsp: ENSP00000441344.1:p.Ser135Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.289A>C
  hgvsp: ENSP00000437667.1:p.Ser97Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.775A>C
  hgvsp: ENSP00000318883.5:p.Ser259Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.291A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*273A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.289A>C
  hgvsp: ENSP00000338932.5:p.Ser97Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*381A>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*45A>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser259Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-18209624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209624
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209624
    reference: chr 22
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*351G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*388G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.298G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.296G>A
  hgvsp: ENSP00000338932.5:p.Ser99Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.782G>A
  hgvsp: ENSP00000318883.5:p.Ser261Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*52G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.410G>A
  hgvsp: ENSP00000441344.1:p.Ser137Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*280G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.296G>A
  hgvsp: ENSP00000437667.1:p.Ser99Asn
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9512
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser261Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-18209628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209628
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209628
    reference: chr 22
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*56G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.300G>A
  hgvsp: ENSP00000437667.1:p.Trp100Ter
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.302G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.300G>A
  hgvsp: ENSP00000338932.5:p.Trp100Ter
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.786G>A
  hgvsp: ENSP00000318883.5:p.Trp262Ter
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*284G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*355G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.414G>A
  hgvsp: ENSP00000441344.1:p.Trp138Ter
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*392G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Trp262Ter
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

22-18209631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209631
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209631
    reference: chr 22
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.417C>T
  hgvsp: ENST00000538149.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.303C>T
  hgvsp: ENST00000337612.5:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.303C>T
  hgvsp: ENST00000543133.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.789C>T
  hgvsp: ENST00000317582.5:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*395C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*358C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*287C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*59C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.305C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His263His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-18209635-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209635
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209635
    reference: chr 22
allele count: 4
allele frequency: 3.297011259293451e-5
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*362G>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.307G>C
  hgvsp: ENSP00000437667.1:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*291G>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.421G>C
  hgvsp: ENSP00000441344.1:p.Glu141Gln
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.309G>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*399G>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.793G>C
  hgvsp: ENSP00000318883.5:p.Glu265Gln
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.307G>C
  hgvsp: ENSP00000338932.5:p.Glu103Gln
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*63G>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11091
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu265Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-18209640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209640
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209640
    reference: chr 22
allele count: 8
allele frequency: 6.59326168655634e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*404C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.312C>T
  hgvsp: ENST00000543133.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*296C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.426C>T
  hgvsp: ENST00000538149.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.798C>T
  hgvsp: ENST00000317582.5:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*68C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.312C>T
  hgvsp: ENST00000337612.5:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*367C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.314C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7887
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser266Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

22-18209646-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209646
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209646
    reference: chr 22
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*373A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*74A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*410A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.432A>G
  hgvsp: ENST00000538149.1:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.804A>G
  hgvsp: ENST00000317582.5:c.804A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*302A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.318A>G
  hgvsp: ENST00000543133.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.318A>G
  hgvsp: ENST00000337612.5:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.320A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro268Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

22-18209651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209651
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209651
    reference: chr 22
allele count: 11
allele frequency: 9.066332586047738e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*307C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.325C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.323C>T
  hgvsp: ENSP00000437667.1:p.Ser108Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.323C>T
  hgvsp: ENSP00000338932.5:p.Ser108Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.437C>T
  hgvsp: ENSP00000441344.1:p.Ser146Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*415C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*378C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.809C>T
  hgvsp: ENSP00000318883.5:p.Ser270Leu
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*79C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9491
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10640
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser270Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

22-18209654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209654
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209654
    reference: chr 22
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.328T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*82T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*418T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.326T>C
  hgvsp: ENSP00000437667.1:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*381T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.812T>C
  hgvsp: ENSP00000318883.5:p.Leu271Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.440T>C
  hgvsp: ENSP00000441344.1:p.Leu147Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.326T>C
  hgvsp: ENSP00000338932.5:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*310T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4365
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu271Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

22-18209662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209662
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209662
    reference: chr 22
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*389G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*318G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*90G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.334G>A
  hgvsp: ENSP00000437667.1:p.Glu112Lys
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.334G>A
  hgvsp: ENSP00000338932.5:p.Glu112Lys
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.448G>A
  hgvsp: ENSP00000441344.1:p.Glu150Lys
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.820G>A
  hgvsp: ENSP00000318883.5:p.Glu274Lys
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*426G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.336G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10606
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu274Lys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

22-18209668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209668
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209668
    reference: chr 22
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.454T>C
  hgvsp: ENSP00000441344.1:p.Trp152Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.826T>C
  hgvsp: ENSP00000318883.5:p.Trp276Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*96T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.340T>C
  hgvsp: ENSP00000338932.5:p.Trp114Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*324T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.340T>C
  hgvsp: ENSP00000437667.1:p.Trp114Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*395T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.342T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*432T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10587
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4385
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp276Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

22-18209673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209673
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209673
    reference: chr 22
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*400G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.459G>A
  hgvsp: ENST00000538149.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*437G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*101G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.347G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.831G>A
  hgvsp: ENST00000317582.5:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.345G>A
  hgvsp: ENST00000337612.5:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.345G>A
  hgvsp: ENST00000543133.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*329G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11080
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln277Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

22-18209700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209700
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209700
    reference: chr 22
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*356G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.372G>A
  hgvsp: ENST00000543133.1:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.858G>A
  hgvsp: ENST00000317582.5:c.858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*464G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.374G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*427G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*128G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.372G>A
  hgvsp: ENST00000337612.5:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.486G>A
  hgvsp: ENST00000538149.1:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val286Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

22-18209711-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209711
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209711
    reference: chr 22
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*438A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*475A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.497A>G
  hgvsp: ENSP00000441344.1:p.Asp166Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.869A>G
  hgvsp: ENSP00000318883.5:p.Asp290Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*139A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*367A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.383A>G
  hgvsp: ENSP00000437667.1:p.Asp128Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.385A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.383A>G
  hgvsp: ENSP00000338932.5:p.Asp128Gly
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp290Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

22-18209718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209718
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209718
    reference: chr 22
allele count: 15045
allele frequency: 1.240783809193924e-1
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.876C>T
  hgvsp: ENST00000317582.5:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*374C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.392C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*482C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.504C>T
  hgvsp: ENST00000538149.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*445C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.390C>T
  hgvsp: ENST00000543133.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.390C>T
  hgvsp: ENST00000337612.5:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*146C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 4.25e1
  variant carriers: 1776
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 6.25e1
  variant carriers: 946
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 9649
  bin: 3.25e1
  variant carriers: 958
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 2.75e1
  variant carriers: 594
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 6220
  bin: 4.75e1
  variant carriers: 1706
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 9.75e1
  variant carriers: 1059
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 303
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 5.75e1
  variant carriers: 1272
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.25e1
  variant carriers: 443
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 1600
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 671
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 3.75e1
  variant carriers: 1511
genotype quality: GenotypeQuality
  all individuals: 3629
  bin: 7.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 11
hgvs: p.Asn292Asn
num of homozygotes: 1196
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

22-18209719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209719
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209719
    reference: chr 22
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.391G>A
  hgvsp: ENSP00000338932.5:p.Gly131Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*483G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*147G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*375G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.391G>A
  hgvsp: ENSP00000437667.1:p.Gly131Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.393G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*446G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.505G>A
  hgvsp: ENSP00000441344.1:p.Gly169Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.877G>A
  hgvsp: ENSP00000318883.5:p.Gly293Arg
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly293Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

22-18209723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209723
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209723
    reference: chr 22
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*487C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.881C>T
  hgvsp: ENSP00000318883.5:p.Ala294Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.509C>T
  hgvsp: ENSP00000441344.1:p.Ala170Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*151C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.395C>T
  hgvsp: ENSP00000437667.1:p.Ala132Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.397C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*379C>T
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.395C>T
  hgvsp: ENSP00000338932.5:p.Ala132Val
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*450C>T
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4494
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala294Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-18209724-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209724
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209724
    reference: chr 22
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.396T>C
  hgvsp: ENST00000543133.1:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*152T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.396T>C
  hgvsp: ENST00000337612.5:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*488T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.510T>C
  hgvsp: ENST00000538149.1:c.510T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.882T>C
  hgvsp: ENST00000317582.5:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.398T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*380T>C
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*451T>C
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4239
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala294Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-18209725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209725
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209725
    reference: chr 22
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*452G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.883G>A
  hgvsp: ENSP00000318883.5:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.511G>A
  hgvsp: ENSP00000441344.1:p.Gly171Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*381G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.397G>A
  hgvsp: ENSP00000338932.5:p.Gly133Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*153G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*489G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.397G>A
  hgvsp: ENSP00000437667.1:p.Gly133Arg
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.399G>A
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5883
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly295Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

22-18209729-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209729
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209729
    reference: chr 22
allele count: 3
allele frequency: 2.473247704001715e-5
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.401A>G
  hgvsp: ENSP00000338932.5:p.Glu134Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.403A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*493A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.887A>G
  hgvsp: ENSP00000318883.5:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*456A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.515A>G
  hgvsp: ENSP00000441344.1:p.Glu172Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.401A>G
  hgvsp: ENSP00000437667.1:p.Glu134Gly
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*157A>G
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*385A>G
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu296Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

22-18209735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18209735
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18209735
    reference: chr 22
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000410019
  ensembl transcript: ENST00000418951
  gene symbol: BCL2L13
  hgvsc: ENST00000418951.2:c.*462G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099968
  ensembl transcript: ENST00000485631
  gene symbol: BCL2L13
  hgvsc: ENST00000485631.1:n.409G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000338932
  ensembl transcript: ENST00000337612
  gene symbol: BCL2L13
  hgvsc: ENST00000337612.5:c.407G>A
  hgvsp: ENSP00000338932.5:p.Ser136Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000437667
  ensembl transcript: ENST00000543133
  gene symbol: BCL2L13
  hgvsc: ENST00000543133.1:c.407G>A
  hgvsp: ENSP00000437667.1:p.Ser136Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000382677
  ensembl transcript: ENST00000399777
  gene symbol: BCL2L13
  hgvsc: ENST00000399777.1:c.*391G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000318883
  ensembl transcript: ENST00000317582
  gene symbol: BCL2L13
  hgvsc: ENST00000317582.5:c.893G>A
  hgvsp: ENSP00000318883.5:p.Ser298Asn
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000436321
  ensembl transcript: ENST00000498133
  gene symbol: BCL2L13
  hgvsc: ENST00000498133.1:c.*499G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000347133
  ensembl transcript: ENST00000355028
  gene symbol: BCL2L13
  hgvsc: ENST00000355028.3:c.*163G>A
  variant of: http://identifiers.org/hgnc/17164
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099968
  ensembl protein: ENSP00000441344
  ensembl transcript: ENST00000538149
  gene symbol: BCL2L13
  hgvsc: ENST00000538149.1:c.521G>A
  hgvsp: ENSP00000441344.1:p.Ser174Asn
  variant of: http://identifiers.org/hgnc/17164
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser298Asn
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 51874
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.226692836113837e-4
allele num: 8152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61432
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 4.393782e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 6.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeQuality
all individuals: 810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51874
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627816121890871e-5
allele num: 61432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.393782e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

FS
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

QD
type: SiteQuality
SIO_000300: 6.27e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeQuality
all individuals: 51874
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.226692836113837e-4
allele num: 8152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.032e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.167e0

VQSLOD
type: SiteQuality
SIO_000300: -1.449e0

FS
type: SiteQuality
SIO_000300: 4.862e0

MQ
type: SiteQuality
SIO_000300: 5.676e1

QD
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 4.393702e6

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 769
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51873
bin: 9.75e1
variant carriers: 6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.511264487563485e-5
allele num: 61432
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21921482565228e-4
allele num: 8202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

QD
type: SiteQuality
SIO_000300: 1.451e1

DP
type: SiteQuality
SIO_000300: 4.393807e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.622e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

GenotypeQuality
all individuals: 768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51876
bin: 9.75e1
variant carriers: 96

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 70
allele frequency: 1.13947128532361e-3
allele num: 61432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.453385672227674e-4
allele num: 8152
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.233197681588359e-3
allele num: 16218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.761493746697199e-4
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.038590094196293e-4
allele num: 6582
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

FS
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.346e0

DP
type: SiteQuality
SIO_000300: 4.396492e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

QD
type: SiteQuality
SIO_000300: 1.264e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51868
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165988407941794e-5
allele num: 16218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61430
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.39265e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.65e0

FS
type: SiteQuality
SIO_000300: 8.239000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

QD
type: SiteQuality
SIO_000300: 1.131e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.91e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 528
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51868
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 768
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.75371860521824e-4
allele num: 8202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.766896731345227e-5
allele num: 61432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.392953e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 1.738e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

QD
type: SiteQuality
SIO_000300: 1.275e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.667e0

GenotypeQuality
all individuals: 794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.453385672227674e-4
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61432
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

QD
type: SiteQuality
SIO_000300: 1.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 1.738e0

DP
type: SiteQuality
SIO_000300: 4.392953e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.667e0

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627869119322807e-5
allele num: 61430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

FS
type: SiteQuality
SIO_000300: 9.247999999999999e0

DP
type: SiteQuality
SIO_000300: 4.392013e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

GenotypeQuality
all individuals: 484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51867
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627975124540097e-5
allele num: 61426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.16e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.669e1

DP
type: SiteQuality
SIO_000300: 4.391663e6

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

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
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GenotypeQuality
all individuals: 227
bin: 2.5e0
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GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 491
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variant carriers: 0

GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.23334977799704e-4
allele num: 16216
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

FS
type: SiteQuality
SIO_000300: 1.898e0

DP
type: SiteQuality
SIO_000300: 4.390711e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.415e0

VQSLOD
type: SiteQuality
SIO_000300: -3.32e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

QD
type: SiteQuality
SIO_000300: 8.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
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variant carriers: 0

GenotypeQuality
all individuals: 468
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variant carriers: 0

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.139582587178068e-4
allele num: 61426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 4.39037e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.083e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.527e1

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7901
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4787
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.387854386847844e-5
allele num: 11922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
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: 842
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.913e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.947e0

VQSLOD
type: SiteQuality
SIO_000300: -2.5e-3

FS
type: SiteQuality
SIO_000300: 1.726e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 2.032754e6

GenotypeQuality
all individuals: 326
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4872
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538745614574998e-5
allele num: 64988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12010
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

DP
type: SiteQuality
SIO_000300: 2.045495e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.127e1

GenotypeQuality
all individuals: 2763
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4296
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5392
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 77
bin: 1.75e1
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GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 132
bin: 4.25e1
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GenotypeQuality
all individuals: 646
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19814
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4907
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4934
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 442
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.139300733646438e-5
allele num: 65154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

DP
type: SiteQuality
SIO_000300: 2.060621e6

QD
type: SiteQuality
SIO_000300: 1.433e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
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SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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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: 12648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.532520076012996e-5
allele num: 65252
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

Other
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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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.962e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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SIO_000300: -8.888e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 2.951013181192209e-4
allele num: 10166
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

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

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

Latino
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allele count: 3
allele frequency: 2.604166666666667e-4
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530409231428484e-5
allele num: 65342
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.727975270479135e-5
allele num: 12940
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 2.07698e6

FS
type: SiteQuality
SIO_000300: 4.24e0

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-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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African
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allele count: 2
allele frequency: 1.961553550411926e-4
allele num: 10196
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13422
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65548
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.084963e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

FS
type: SiteQuality
SIO_000300: 1.3301e1

QD
type: SiteQuality
SIO_000300: 1.031e1

VQSLOD
type: SiteQuality
SIO_000300: -9.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
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: 11526
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 2.989e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.019e0

QD
type: SiteQuality
SIO_000300: 1.068e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.087444e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.615218252155107e-5
allele num: 65658
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13774
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

East Asian
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.265e0

DP
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BaseQRankSum
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SIO_000300: 1.32e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.507567991316408e-5
allele num: 66332
num of homozygotes: 0

South Asian
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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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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variant carriers: 0

African
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allele count: 0
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allele num: 10320
num of homozygotes: 0

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: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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Other
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allele num: 900
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South Asian
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Latino
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num of homozygotes: 0

FS
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
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allele count: 1
allele frequency: 6.180469715698394e-5
allele num: 16180
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European (Finnish)
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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: 10332
num of homozygotes: 0

Latino
type: Population
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: 66486
num of homozygotes: 0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
type: SiteQuality
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.02e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

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

Other
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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: 16180
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.109e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 1.2e-3

QD
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SIO_000300: 1.31e1

ClippingRankSum
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SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-1

BaseQRankSum
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SIO_000300: 4.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.129864e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

DP
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SIO_000300: 2.131191e6

BaseQRankSum
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SIO_000300: -3.213e0

MQRankSum
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SIO_000300: 3.38e-1

ClippingRankSum
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QD
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SIO_000300: 9.85e0

FS
type: SiteQuality
SIO_000300: 9.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66580
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

MQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

QD
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SIO_000300: 1.34e1

DP
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.51e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
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SIO_000300: 1.72e0

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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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.979e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: -3.259e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.137672e6

QD
type: SiteQuality
SIO_000300: 1.219e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.162e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
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South Asian
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allele frequency: 0.0e0
allele num: 16490
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.0143e1

ReadPosRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.03e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.414e1

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: 0

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 1.199580146948568e-3
allele num: 66690
num of homozygotes: 0

Latino
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allele frequency: 1.296008294453084e-3
allele num: 11574
num of homozygotes: 0

African
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allele count: 168
allele frequency: 1.614763552479815e-2
allele num: 10404
num of homozygotes: 3

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

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

Other
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allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.151534e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

VQSLOD
type: SiteQuality
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66710
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Latino
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South Asian
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
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SIO_000300: -4.97e-1

FS
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SIO_000300: 5.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.46e-1

QD
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SIO_000300: 1.236e1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -2.013e-1

QD
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ClippingRankSum
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SIO_000300: 6.39e-1

ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 9.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.65e-1

BaseQRankSum
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SIO_000300: 3.89e0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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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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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16512
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Latino
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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Other
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Latino
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South 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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ReadPosRankSum
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DP
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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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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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: 16512
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e0

FS
type: SiteQuality
SIO_000300: 1.594e0

VQSLOD
type: SiteQuality
SIO_000300: -4.544e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.436e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e0

DP
type: SiteQuality
SIO_000300: 2.147111e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e0

QD
type: SiteQuality
SIO_000300: 1.436e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 1.594e0

VQSLOD
type: SiteQuality
SIO_000300: -4.544e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.147111e6

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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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.564e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 6.73e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.147155e6

GenotypeQuality
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bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 10
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.855e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.21e-1

FS
type: SiteQuality
SIO_000300: 1.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.881e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

DP
type: SiteQuality
SIO_000300: 2.147382e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6161
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.643e0

DP
type: SiteQuality
SIO_000300: 2.14723e6

VQSLOD
type: SiteQuality
SIO_000300: -9.829e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.25e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.51e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.14661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

QD
type: SiteQuality
SIO_000300: 2.133e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 38

GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.64558669264199e-4
allele num: 66730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

DP
type: SiteQuality
SIO_000300: 2.147461e6

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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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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MQRankSum
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DP
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FS
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

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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bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.18e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 1.271e0

DP
type: SiteQuality
SIO_000300: 2.148302e6

QD
type: SiteQuality
SIO_000300: 1.422e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 55

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 19

GenotypeQuality
all individuals: 3055
bin: 6.25e1
variant carriers: 119

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 844
bin: 7.25e1
variant carriers: 129

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 31

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 43

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 12

GenotypeQuality
all individuals: 1470
bin: 6.75e1
variant carriers: 136

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 61

GenotypeQuality
all individuals: 1051
bin: 9.25e1
variant carriers: 358

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 12

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 29

GenotypeQuality
all individuals: 50533
bin: 9.75e1
variant carriers: 47977

GenotypeQuality
all individuals: 702
bin: 8.75e1
variant carriers: 188

European (Non-Finnish)
type: Population
allele count: 34829
allele frequency: 5.22848049959468e-1
allele num: 66614
num of homozygotes: 9159

Other
type: Population
allele count: 548
allele frequency: 6.035242290748899e-1
allele num: 908
num of homozygotes: 168

African
type: Population
allele count: 6259
allele frequency: 6.021743313450068e-1
allele num: 10394
num of homozygotes: 1895

South Asian
type: Population
allele count: 10538
allele frequency: 6.385118759088706e-1
allele num: 16504
num of homozygotes: 3380

Latino
type: Population
allele count: 8079
allele frequency: 7.000866551126517e-1
allele num: 11540
num of homozygotes: 2806

East Asian
type: Population
allele count: 8059
allele frequency: 9.318917668825162e-1
allele num: 8648
num of homozygotes: 3754

European (Finnish)
type: Population
allele count: 3368
allele frequency: 5.099939430648092e-1
allele num: 6604
num of homozygotes: 846

BaseQRankSum
type: SiteQuality
SIO_000300: -8.05e-1

DP
type: SiteQuality
SIO_000300: 3.330986e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.21e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

QD
type: SiteQuality
SIO_000300: 2.339e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4760
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6208
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.452e0

DP
type: SiteQuality
SIO_000300: 2.355343e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21331
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4363
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2835
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.49e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.351708e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

GenotypeQuality
all individuals: 21322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4337
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.188e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

DP
type: SiteQuality
SIO_000300: 2.350192e6

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 2.656e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

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

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3704
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4336
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21316
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6125
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
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: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.51e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.916e-1

DP
type: SiteQuality
SIO_000300: 2.348728e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 7.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4667
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6127
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21307
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.886836027713626e-4
allele num: 10392
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.436e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.347846e6

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
all individuals: 3621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4351
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 12742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
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GenotypeQuality
all individuals: 6166
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GenotypeQuality
all individuals: 21311
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3708
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.094357076780758e-4
allele num: 8648
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.349021e6

QD
type: SiteQuality
SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.798e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

GenotypeQuality
all individuals: 6170
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 168
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4667
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3635
bin: 7.25e1
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GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
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GenotypeQuality
all individuals: 104
bin: 2.75e1
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GenotypeQuality
all individuals: 2833
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3707
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21308
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.503e0

MQRankSum
type: SiteQuality
SIO_000300: -1.402e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.739e1

DP
type: SiteQuality
SIO_000300: 2.348314e6

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: 0

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

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199364336901442e-4
allele num: 66702
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: -4.198e0

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

African
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allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.056e0

ReadPosRankSum
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SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.074e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 2.348111e6

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: -1.448e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.347952e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

African
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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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num of homozygotes: 0

Other
type: Population
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.661e-1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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FS
type: SiteQuality
SIO_000300: 6.553e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.348879e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10772
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variant carriers: 11

European (Finnish)
type: Population
allele count: 1202
allele frequency: 1.820109024833434e-1
allele num: 6604
num of homozygotes: 110

Other
type: Population
allele count: 110
allele frequency: 1.214128035320088e-1
allele num: 906
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European (Non-Finnish)
type: Population
allele count: 11097
allele frequency: 1.66496624156039e-1
allele num: 66650
num of homozygotes: 954

East Asian
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allele count: 54
allele frequency: 6.25e-3
allele num: 8640
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South Asian
type: Population
allele count: 913
allele frequency: 5.529312015503876e-2
allele num: 16512
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Latino
type: Population
allele count: 1374
allele frequency: 1.18919854595811e-1
allele num: 11554
num of homozygotes: 83

African
type: Population
allele count: 295
allele frequency: 2.839815171351559e-2
allele num: 10388
num of homozygotes: 5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.557471e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

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

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 66674
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
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: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.294e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

MQRankSum
type: SiteQuality
SIO_000300: 7.12e-1

FS
type: SiteQuality
SIO_000300: 3.001e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

DP
type: SiteQuality
SIO_000300: 2.390884e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5900
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22406
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.103e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.14e-1

QD
type: SiteQuality
SIO_000300: 8.17e0

DP
type: SiteQuality
SIO_000300: 2.390342e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 2724
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12861
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variant carriers: 0

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

GenotypeQuality
all individuals: 143
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 3694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.069e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

DP
type: SiteQuality
SIO_000300: 2.39045e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.642e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3694
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3407
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.192e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.390294e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.284e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.566e0

MQRankSum
type: SiteQuality
SIO_000300: -4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

GenotypeQuality
all individuals: 4488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12691
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 3698
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22406
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.594258042199931e-4
allele num: 11564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.049e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e0

QD
type: SiteQuality
SIO_000300: 2.082e1

VQSLOD
type: SiteQuality
SIO_000300: -2.678e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.390116e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

FS
type: SiteQuality
SIO_000300: 6.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1