16-3117655-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117655
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117655
    reference: chr 16
allele count: 1
allele frequency: 8.768237934904602e-6
allele num: 114048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.370G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+239G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+239G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+239G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.346G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+41G>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/16-3117658-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117658
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117658
    reference: chr 16
allele count: 1
allele frequency: 8.804211934989699e-6
allele num: 113582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+242C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.753C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.349C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+242C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.373C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+242C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+242C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+44C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+44C>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

16-3117658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117658
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117658
    reference: chr 16
allele count: 1
allele frequency: 8.804211934989699e-6
allele num: 113582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.753C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+242C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+242C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.373C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+44C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+242C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-3117661-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117661
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117661
    reference: chr 16
allele count: 1
allele frequency: 8.813834194151139e-6
allele num: 113458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+245A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.376A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.352A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+245A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+245A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+245A>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+47A>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-3117665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117665
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117665
    reference: chr 16
allele count: 339
allele frequency: 3.003136018142839e-3
allele num: 112882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+249A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.380A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+249A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+249A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+51A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.356A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.760A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+51A>G
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 4
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-3117667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117667
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117667
    reference: chr 16
allele count: 23
allele frequency: 2.043536206130609e-4
allele num: 112550
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.762T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.358T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+251T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+251T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.382T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+251T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+251T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+53T>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-3117667-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117667
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117667
    reference: chr 16
allele count: 1
allele frequency: 8.88494002665482e-6
allele num: 112550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.358T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+251T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+251T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+251T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+251T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.382T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.762T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+53T>G
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/16-3117669-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117669
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117669
    reference: chr 16
allele count: 4
allele frequency: 3.564490545188829e-5
allele num: 112218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.764C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.384C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.360C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+253C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+55C>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

16-3117669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117669
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117669
    reference: chr 16
allele count: 3
allele frequency: 2.673367908891622e-5
allele num: 112218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+253C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.764C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+253C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.360C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+253C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.384C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+55C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

16-3117675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117675
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117675
    reference: chr 16
allele count: 1
allele frequency: 8.997012991686761e-6
allele num: 111148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.390G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+259G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+259G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+259G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.366G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.770G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+61G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+61G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD

16-3117675-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117675
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117675
    reference: chr 16
allele count: 108
allele frequency: 9.7167740310217e-4
allele num: 111148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+259G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.366G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.390G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.770G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+259G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+61G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+61G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 2
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

16-3117678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117678
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117678
    reference: chr 16
allele count: 2
allele frequency: 1.809790969143064e-5
allele num: 110510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.369T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.393T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+262T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+262T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.773T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+64T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+262T>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-3117679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117679
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117679
    reference: chr 16
allele count: 1
allele frequency: 9.085292728131701e-6
allele num: 110068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.370G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.394G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+263G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.774G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+263G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+65G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+263G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+263G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+65G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-3117680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117680
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117680
    reference: chr 16
allele count: 4
allele frequency: 3.634777551613841e-5
allele num: 110048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+264G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.371G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.395G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.775G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+264G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+264G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+66G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+264G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-3117680-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117680
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117680
    reference: chr 16
allele count: 1
allele frequency: 9.086943879034603e-6
allele num: 110048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+264G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.371G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+264G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.775G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.395G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+66G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+264G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-3117681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117681
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117681
    reference: chr 16
allele count: 8
allele frequency: 7.300735549106573e-5
allele num: 109578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+265G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+265G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+265G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.372G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+265G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.396G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.776G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+67G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-3117682-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117682
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117681
    reference: chr 16
allele count: 3
allele frequency: 2.739275735495535e-5
allele num: 109518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+267delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.398delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+267delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+267delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.374delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.778delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+267delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+69delC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+69delC
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: GC
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-3117683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117683
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117683
    reference: chr 16
allele count: 1
allele frequency: 9.159186664224217e-6
allele num: 109180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+267C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.374C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.398C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+267C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.778C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+69C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/16-3117685-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117685
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117685
    reference: chr 16
allele count: 3
allele frequency: 2.757606397646843e-5
allele num: 108790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+269C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.780C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+269C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.400C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.376C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+71C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+71C>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

16-3117687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117687
    reference: chr 16
allele count: 1
allele frequency: 9.253090532237768e-6
allele num: 108072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+271G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.378G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.402G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+271G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.782G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+271G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+73G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+271G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

16-3117687-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117687
    reference: chr 16
allele count: 1
allele frequency: 9.253090532237768e-6
allele num: 108072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+271G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+271G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+271G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.402G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.782G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.378G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+73G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+73G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

16-3117690-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117690
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117690
    reference: chr 16
allele count: 1
allele frequency: 9.368910208364564e-6
allele num: 106736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.381T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+274T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.785T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+274T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.405T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+274T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+76T>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

16-3117693-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117693
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117693
    reference: chr 16
allele count: 3
allele frequency: 2.836986741815293e-5
allele num: 105746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.788G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.384G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.408G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+277G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+79G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+277G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

16-3117696-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117696
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117696
    reference: chr 16
allele count: 1
allele frequency: 9.588279287399084e-6
allele num: 104294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+280G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.791G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.411G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+280G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+280G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+82G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.387G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-3117698-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117698
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117698
    reference: chr 16
allele count: 1
allele frequency: 9.588830929733047e-6
allele num: 104288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.54+282A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.54+282A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.54+282A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+282A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.793A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.389A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.413A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.54+282A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+84A>G
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

16-3117703-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117703
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117703
    reference: chr 16
allele count: 1
allele frequency: 9.734823410303337e-6
allele num: 102724
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-282G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.798G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-282G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-282G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.418G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.394G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+89G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+89G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-3117703-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117703
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117703
    reference: chr 16
allele count: 84
allele frequency: 8.177251664654803e-4
allele num: 102724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-282G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-282G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.418G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.798G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-282G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+287G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.394G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+89G>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-3117704-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117704
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117704
    reference: chr 16
allele count: 1
allele frequency: 9.896678674636792e-6
allele num: 101044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-281A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.395A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.799A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-281A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-281A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.419A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+90A>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+288A>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

16-3117705-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117705
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117705
    reference: chr 16
allele count: 6
allele frequency: 5.941535292719638e-5
allele num: 100984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.420G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-280G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-280G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-280G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.396G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+289G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+91G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

16-3117706-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117706
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117706
    reference: chr 16
allele count: 11
allele frequency: 1.090080269547121e-4
allele num: 100910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.421G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-279G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.801G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-279G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-279G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.397G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+92G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+92G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

16-3117707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117707
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117707
    reference: chr 16
allele count: 1
allele frequency: 9.909427829637117e-6
allele num: 100914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+291G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-278G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.422G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-278G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.398G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-278G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.802G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+93G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

16-3117709-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117709
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117709
    reference: chr 16
allele count: 1
allele frequency: 1.006380452066099e-5
allele num: 99366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.424C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+293C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.400C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-276C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-276C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-276C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.804C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+95C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+95C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

16-3117716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117716
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117716
    reference: chr 16
allele count: 1
allele frequency: 1.020428988346701e-5
allele num: 97998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-269G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.811G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.431G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-269G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.407G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-269G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+102G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

16-3117716-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117716
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117716
    reference: chr 16
allele count: 281
allele frequency: 2.86740545725423e-3
allele num: 97998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-269G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-269G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.431G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.407G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.811G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+102G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 4
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

16-3117718-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117718
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117719
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 97424
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-264dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-264dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.816dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-264dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.412dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-264dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.436dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+107dupC
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+107dupC
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-3117719-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117719
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117719
    reference: chr 16
allele count: 40
allele frequency: 4.132146030040701e-4
allele num: 96802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-266C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.434C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-266C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.814C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-266C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.410C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+105C>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-3117722-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117722
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117722
    reference: chr 16
allele count: 1
allele frequency: 1.041666666666667e-5
allele num: 96000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.413T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.437T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.817T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-263T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-263T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-263T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+108T>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-263T>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-3117723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117723
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117723
    reference: chr 16
allele count: 5
allele frequency: 5.264487870619946e-5
allele num: 94976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-262C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-262C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-262C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.414C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.818C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+109C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.438C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+307C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/16-3117725-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117725
    reference: chr 16
allele count: 4
allele frequency: 4.228687415426252e-5
allele num: 94592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.416C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-260C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.820C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.440C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+111C>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+111C>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

16-3117727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117727
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117727
    reference: chr 16
allele count: 1
allele frequency: 1.066257223892692e-5
allele num: 93786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.822C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-258C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.442C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.252+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.418C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-258C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+113C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+113C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

16-3117733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117733
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117733
    reference: chr 16
allele count: 1
allele frequency: 1.096058573370161e-5
allele num: 91236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.448C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-252C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-252C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-252C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.424C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.828C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-252C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.252+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+119C>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+119C>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-3117734-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117734
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117734
    reference: chr 16
allele count: 5
allele frequency: 5.559756260285549e-5
allele num: 89932
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-251G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.449G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.425G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-251G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.829G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-251G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-251G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+120G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

16-3117738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117738
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117738
    reference: chr 16
allele count: 351
allele frequency: 4.07060351625922e-3
allele num: 86228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.429G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.453G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-247G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-247G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.833G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.54+322G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.114+124G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 8
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

16-3117739-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117739
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117739
    reference: chr 16
allele count: 1
allele frequency: 1.15077447121913e-5
allele num: 86898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-246C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532086
  gene symbol: IL32
  hgvsc: ENST00000532086.1:n.834C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.252+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.84+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.454C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.252+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.186+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-246C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-246C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000534748
  gene symbol: IL32
  hgvsc: ENST00000534748.2:n.430C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.114+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.252+125C>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.252+125C>G
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

16-3117936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117936
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117936
    reference: chr 16
allele count: 2
allele frequency: 1.651145895251304e-5
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.132G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.253-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-245G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.253-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-245G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.651G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.115-49G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.55-245G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-49G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-3117936-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117936
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117936
    reference: chr 16
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-245G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.651G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.115-245G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-245G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.132G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.115-49G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.253-49G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-3117937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117937
    reference: chr 16
allele count: 73356
allele frequency: 6.078554855817037e-1
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.652G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-244G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.55-244G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-244G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.115-244G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.133G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.115-48G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-48G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 22644
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-3117938-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117938
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117938
    reference: chr 16
allele count: 2
allele frequency: 1.651091371396493e-5
allele num: 121132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.115-243G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-243G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.134G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.253-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-47G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.653G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-47G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

16-3117938-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117938
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117938
    reference: chr 16
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.253-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-243G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.134G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.253-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-243G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.55-243G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.653G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-47G>T
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.115-47G>T
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-3117943-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117943
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117943
    reference: chr 16
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.253-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.139G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.253-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-238G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.658G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.115-42G>C
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-238G>C
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

16-3117944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117944
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117944
    reference: chr 16
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447812
  ensembl transcript: ENST00000549213
  gene symbol: IL32
  hgvsc: ENST00000549213.1:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449147
  ensembl transcript: ENST00000551513
  gene symbol: IL32
  hgvsc: ENST00000551513.1:c.253-237A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.659A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.140A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.253-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.115-237A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448683
  ensembl transcript: ENST00000552664
  gene symbol: IL32
  hgvsc: ENST00000552664.1:c.115-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-41A>G
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-237A>G
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-3117944-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117944
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117943
    reference: chr 16
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000532247
  gene symbol: IL32
  hgvsc: ENST00000532247.1:n.661delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-235delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380099
  ensembl transcript: ENST00000396890
  gene symbol: IL32
  hgvsc: ENST00000396890.2:c.253-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000437020
  ensembl transcript: ENST00000529550
  gene symbol: IL32
  hgvsc: ENST00000529550.1:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000448354
  ensembl transcript: ENST00000548807
  gene symbol: IL32
  hgvsc: ENST00000548807.1:c.253-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.253-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.142delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431775
  ensembl transcript: ENST00000534507
  gene symbol: IL32
  hgvsc: ENST00000534507.1:c.253-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.55-235delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446624
  ensembl transcript: ENST00000548652
  gene symbol: IL32
  hgvsc: ENST00000548652.1:c.115-235delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436929
  ensembl transcript: ENST00000530538
  gene symbol: IL32
  hgvsc: ENST00000530538.2:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.115-39delG
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: AG
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-3117945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3117945
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 3117945
    reference: chr 16
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433747
  ensembl transcript: ENST00000530890
  gene symbol: IL32
  hgvsc: ENST00000530890.1:c.55-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433866
  ensembl transcript: ENST00000525377
  gene symbol: IL32
  hgvsc: ENST00000525377.2:c.253-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447979
  ensembl transcript: ENST00000548246
  gene symbol: IL32
  hgvsc: ENST00000548246.1:c.55-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447496
  ensembl transcript: ENST00000551122
  gene symbol: IL32
  hgvsc: ENST00000551122.1:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000371648
  ensembl transcript: ENST00000382213
  gene symbol: IL32
  hgvsc: ENST00000382213.3:c.115-236G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000449483
  ensembl transcript: ENST00000548476
  gene symbol: IL32
  hgvsc: ENST00000548476.1:c.253-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000433177
  ensembl transcript: ENST00000531965
  gene symbol: IL32
  hgvsc: ENST00000531965.1:c.85-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000405063
  ensembl transcript: ENST00000440815
  gene symbol: IL32
  hgvsc: ENST00000440815.3:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432850
  ensembl transcript: ENST00000528163
  gene symbol: IL32
  hgvsc: ENST00000528163.2:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000447033
  ensembl transcript: ENST00000552936
  gene symbol: IL32
  hgvsc: ENST00000552936.1:c.187-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432218
  ensembl transcript: ENST00000525643
  gene symbol: IL32
  hgvsc: ENST00000525643.2:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000450364
  ensembl transcript: ENST00000526464
  gene symbol: IL32
  hgvsc: ENST00000526464.2:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000432917
  ensembl transcript: ENST00000533097
  gene symbol: IL32
  hgvsc: ENST00000533097.2:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000446978
  ensembl transcript: ENST00000552356
  gene symbol: IL32
  hgvsc: ENST00000552356.1:c.55-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000411958
  ensembl transcript: ENST00000444393
  gene symbol: IL32
  hgvsc: ENST00000444393.3:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000380096
  ensembl transcript: ENST00000396887
  gene symbol: IL32
  hgvsc: ENST00000396887.3:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008517
  ensembl transcript: ENST00000528652
  gene symbol: IL32
  hgvsc: ENST00000528652.2:n.141G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000436937
  ensembl transcript: ENST00000529699
  gene symbol: IL32
  hgvsc: ENST00000529699.1:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000008180
  ensembl transcript: ENST00000008180
  gene symbol: IL32
  hgvsc: ENST00000008180.9:c.55-40G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000431740
  ensembl transcript: ENST00000525228
  gene symbol: IL32
  hgvsc: ENST00000525228.1:c.55-236G>A
  variant of: http://identifiers.org/hgnc/16830
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008517
  ensembl protein: ENSP00000324742
  ensembl transcript: ENST00000325568
  gene symbol: IL32
  hgvsc: ENST00000325568.5:c.115-40G>A
  variant of: http://identifiers.org/hgnc/16830
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: G

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+239G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+239G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+41G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000008517
ensembl transcript: ENST00000532086
gene symbol: IL32
hgvsc: ENST00000532086.1:n.750G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+41G>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 2673
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 805
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14151
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7179
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2530
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28297
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 641
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3009
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 575
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556807921038702e-5
allele num: 64234
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

DP
type: SiteQuality
SIO_000300: 1.620801e6

QD
type: SiteQuality
SIO_000300: 1.237e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.254e0

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+242C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+44C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+44C>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 579
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3188
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28201
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14061
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2725
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7157
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2472
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36333
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.75e1
variant carriers: 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: 9936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562011871290222e-5
allele num: 64020
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12406
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.309e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

FS
type: SiteQuality
SIO_000300: 1.458e0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 1.613364e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000008517
ensembl transcript: ENST00000534748
gene symbol: IL32
hgvsc: ENST00000534748.2:n.349C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+242C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+44C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+242C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+44C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 579
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3188
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7157
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28201
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14061
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2472
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2725
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36333
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4657
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
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: 1
allele frequency: 1.562011871290222e-5
allele num: 64020
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.458e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 1.613364e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000008517
ensembl transcript: ENST00000532086
gene symbol: IL32
hgvsc: ENST00000532086.1:n.756A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+245A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+47A>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 557
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2436
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2711
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3249
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14019
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28236
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 606
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7196
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4798
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36609
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 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: 9942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.19047619047619e-4
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12328
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.569e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.611103e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.184e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.133e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+249A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+249A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+51A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+51A>G
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 3410
bin: 7.5e0
variant carriers: 13

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 5

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 4

GenotypeDepth
all individuals: 28108
bin: 2.75e1
variant carriers: 17

GenotypeDepth
all individuals: 557
bin: 1.75e1
variant carriers: 14

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 12

GenotypeDepth
all individuals: 13888
bin: 3.25e1
variant carriers: 27

GenotypeDepth
all individuals: 766
bin: 4.25e1
variant carriers: 32

GenotypeDepth
all individuals: 2420
bin: 3.75e1
variant carriers: 41

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 70
bin: 6.25e1
variant carriers: 22

GenotypeDepth
all individuals: 717
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7141
bin: 2.25e1
variant carriers: 12

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 39

GenotypeDepth
all individuals: 362
bin: 4.75e1
variant carriers: 41

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 122
bin: 5.75e1
variant carriers: 27

GenotypeDepth
all individuals: 2794
bin: 1.25e1
variant carriers: 19

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9291
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2181
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1462
bin: 9.75e1
variant carriers: 329

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1999
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 939
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36187
bin: 6.25e1
variant carriers: 1

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: 18
allele frequency: 2.824858757062147e-4
allele num: 63720
num of homozygotes: 0

South Asian
type: Population
allele count: 108
allele frequency: 8.925619834710744e-3
allele num: 12100
num of homozygotes: 2

African
type: Population
allele count: 196
allele frequency: 1.982200647249191e-2
allele num: 9888
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.406469760900141e-3
allele num: 11376
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.207729468599034e-3
allele num: 828
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

DP
type: SiteQuality
SIO_000300: 1.602472e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

QD
type: SiteQuality
SIO_000300: 1.292e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+251T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+53T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+53T>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 150
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28169
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 546
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3480
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2841
bin: 1.25e1
variant carriers: 4

GenotypeDepth
all individuals: 2380
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 807
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7126
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 325
bin: 4.75e1
variant carriers: 6

GenotypeDepth
all individuals: 740
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2006
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 2175
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 1.842237481158935e-3
allele num: 11942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.048e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.443e1

DP
type: SiteQuality
SIO_000300: 1.59213e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+251T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+53T>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+53T>G
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3480
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2841
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2380
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28169
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13877
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 807
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7126
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9330
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572425938738285e-5
allele num: 63596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 2.048e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 1.443e1

DP
type: SiteQuality
SIO_000300: 1.59213e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+253C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+253C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+253C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+253C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+55C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+55C>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 7104
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 731
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13825
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3556
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28115
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 870
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2863
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2365
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9307
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5189
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36123
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.302190011028833e-5
allele num: 63470
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.158e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.202e1

DP
type: SiteQuality
SIO_000300: 1.587662e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+253C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.54+253C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+55C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 870
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2365
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 549
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7104
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 731
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28115
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3556
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13825
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2863
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36123
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5189
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 264
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9307
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.726642508271624e-5
allele num: 63470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11766
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.032e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.587662e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.158e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+259G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+259G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.114+61G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3847
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 310
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1154
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27772
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13512
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2275
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 709
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3078
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7110
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35841
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.771929824561403e-5
allele num: 11400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62992
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.568714e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.649e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+259G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+259G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+259G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+61G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+61G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 13512
bin: 3.25e1
variant carriers: 5

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 4

GenotypeDepth
all individuals: 2275
bin: 3.75e1
variant carriers: 14

GenotypeDepth
all individuals: 3078
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27772
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1154
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 6.75e1
variant carriers: 5

GenotypeDepth
all individuals: 709
bin: 4.25e1
variant carriers: 22

GenotypeDepth
all individuals: 528
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 310
bin: 4.75e1
variant carriers: 14

GenotypeDepth
all individuals: 3847
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 11
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 49
bin: 6.25e1
variant carriers: 7

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 5.25e1
variant carriers: 9

GenotypeDepth
all individuals: 7110
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35841
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5696
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9106
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 9.75e1
variant carriers: 106

GenotypeQuality
all individuals: 2110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.385964912280702e-4
allele num: 11400
num of homozygotes: 0

East Asian
type: Population
allele count: 100
allele frequency: 1.205690860863275e-2
allele num: 8294
num of homozygotes: 2

African
type: Population
allele count: 2
allele frequency: 2.046663937781416e-4
allele num: 9772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.228501228501228e-3
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62992
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

DP
type: SiteQuality
SIO_000300: 1.568714e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.649e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+262T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+262T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+64T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+64T>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 27553
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2232
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3998
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1312
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7059
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13327
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 555
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1041
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 912
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.775568181818182e-4
allele num: 11264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62712
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.294e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.665e0

DP
type: SiteQuality
SIO_000300: 1.554358e6

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+263G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+65G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 7027
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3507
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1404
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13195
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 599
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2219
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27302
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 312
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.600153614747016e-5
allele num: 62494
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.729e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.456e-1

FS
type: SiteQuality
SIO_000300: 2.981e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.545706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+264G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+66G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+66G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4117
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 582
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2207
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13155
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7050
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27326
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1408
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3513
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 330
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.917424647761727e-5
allele num: 11214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.801382798245895e-5
allele num: 62482
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.544857e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 1.345e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+264G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+66G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+264G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+66G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 3513
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13155
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27326
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4117
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2207
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 582
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1408
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7050
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 35193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62482
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.025270758122743e-5
allele num: 11080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.345e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

DP
type: SiteQuality
SIO_000300: 1.544857e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+265G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+67G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+67G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 7037
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27053
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2185
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4227
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 281
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 13000
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 674
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3725
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6350
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 8822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.313951362223441e-4
allele num: 10938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62270
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.534881e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.433e1

FS
type: SiteQuality
SIO_000300: 3.031e0

MQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+267delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+69delC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+69delC
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 1529
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7066
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3716
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12966
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 611
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 675
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27063
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2176
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4249
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 276
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1020
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.821445790877825e-5
allele num: 62222
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.533993e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

QD
type: SiteQuality
SIO_000300: 1.481e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 4.252e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.486e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.8e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+267C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+267C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+69C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+267C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+69C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 663
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26968
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1584
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4315
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2163
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12839
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7088
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3806
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34661
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6545
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610669071932481e-5
allele num: 62086
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.121e0

MQRankSum
type: SiteQuality
SIO_000300: -4.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
SIO_000300: 4.304e0

QD
type: SiteQuality
SIO_000300: 1.425e1

DP
type: SiteQuality
SIO_000300: 1.528657e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+269C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+269C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+71C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+269C>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1703
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26733
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4438
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4018
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12633
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7077
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2138
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8710
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.115264797507788e-4
allele num: 9630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.37e-1

DP
type: SiteQuality
SIO_000300: 1.518606e6

FS
type: SiteQuality
SIO_000300: 7.14e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.566e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+271G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+73G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4443
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12247
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1881
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4621
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7065
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 637
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26318
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 273
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.625276296970485e-5
allele num: 61528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10538
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

DP
type: SiteQuality
SIO_000300: 1.499786e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.465e0

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 1.139e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+271G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+271G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+73G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 637
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7065
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12247
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26318
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4443
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4621
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1881
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 273
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.489466691971911e-5
allele num: 10538
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

DP
type: SiteQuality
SIO_000300: 1.499786e6

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.465e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 5.922e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+274T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+274T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+76T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+76T>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 6902
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2178
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5242
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25439
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11720
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1008
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4924
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1991
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 618
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8099
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 990
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 942
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7890
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60888
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.259763164525069e-4
allele num: 7938
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.144e0

QD
type: SiteQuality
SIO_000300: 1.268e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 1.467867e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.88e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.54+277G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+277G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.54+277G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+79G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 6910
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2395
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5176
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5775
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1916
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11216
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 24832
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 260
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 606
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1052
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.963271788763152e-5
allele num: 60444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.545e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.558e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.443727e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 3.179e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.54+280G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.54+280G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+82G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+82G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5528
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10423
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1800
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2720
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 600
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6842
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23760
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6816
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29438
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2867
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 812
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.303101381287464e-4
allele num: 7674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59776
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.404284e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.297e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.094e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -8.743e-1

QD
type: SiteQuality
SIO_000300: 1.927e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+84A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+84A>G
variant of: http://identifiers.org/hgnc/16830

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

GenotypeDepth
all individuals: 6793
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2742
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23778
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5570
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10266
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1775
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1471
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6997
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7318
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.67319211591875e-5
allele num: 59766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: 5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.401753e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+287G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.114+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+89G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-282G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 40
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6625
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1950
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5934
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 579
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3114
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9613
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22170
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1711
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8265
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 446
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1694
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27965
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.331203407880724e-4
allele num: 7512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.355193e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.271e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-282G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+89G>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1711
bin: 3.75e1
variant carriers: 12

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22170
bin: 2.75e1
variant carriers: 14

GenotypeDepth
all individuals: 8265
bin: 1.25e1
variant carriers: 6

GenotypeDepth
all individuals: 5934
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 1950
bin: 1.75e1
variant carriers: 7

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 6625
bin: 2.25e1
variant carriers: 12

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3114
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 123
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 579
bin: 4.25e1
variant carriers: 6

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9613
bin: 3.25e1
variant carriers: 15

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 82
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10462
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.75e1
variant carriers: 85

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27965
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.695892548248143e-5
allele num: 58966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.045150501672241e-4
allele num: 9568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

East Asian
type: Population
allele count: 82
allele frequency: 1.091586794462194e-2
allele num: 7512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

QD
type: SiteQuality
SIO_000300: 1.271e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.355193e6

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-281A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+90A>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+90A>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20140
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6219
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1566
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8539
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3544
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10325
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2715
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2450
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.721466689619556e-5
allele num: 58090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 3.245e0

QD
type: SiteQuality
SIO_000300: 1.204e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.23e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.292925e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.301e0

VQSLOD
type: SiteQuality
SIO_000300: -1.18e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+91G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.55-280G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000008517
ensembl transcript: ENST00000532086
gene symbol: IL32
hgvsc: ENST00000532086.1:n.800G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+91G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 1551
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 10316
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6372
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6230
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20166
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2704
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3557
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8468
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 966
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 675
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3675
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11508
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.936808846761453e-4
allele num: 10128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.722949689869056e-5
allele num: 58040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

FS
type: SiteQuality
SIO_000300: 2.009e0

QD
type: SiteQuality
SIO_000300: 1.086e1

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

DP
type: SiteQuality
SIO_000300: 1.29176e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+290G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+92G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-279G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+92G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 10315
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3566
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6256
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20216
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1539
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6430
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2680
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 79
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8367
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1444
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.896290166873535e-4
allele num: 58008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.075e0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

DP
type: SiteQuality
SIO_000300: 1.290226e6

QD
type: SiteQuality
SIO_000300: 1.321e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.55-278G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+93G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+93G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 2666
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6493
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 552
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6279
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20221
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10319
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8288
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3586
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11706
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25707
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9084
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.073652566029633e-4
allele num: 9314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.356e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.668e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.043e0

DP
type: SiteQuality
SIO_000300: 1.288523e6

MQRankSum
type: SiteQuality
SIO_000300: 9.64e-1

QD
type: SiteQuality
SIO_000300: 1.578e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+95C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-276C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 537
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1414
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6261
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7341
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3643
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12096
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6491
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18110
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3975
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1598
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4086
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21958
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4908
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8946
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.100352112676056e-4
allele num: 9088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.134e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

DP
type: SiteQuality
SIO_000300: 1.231469e6

FS
type: SiteQuality
SIO_000300: 3.468e0

QD
type: SiteQuality
SIO_000300: 1.107e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+300G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-269G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+102G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 13867
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4412
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4750
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6286
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6746
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15953
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6010
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1291
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4089
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20606
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13291
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.602564102564103e-4
allele num: 6240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.265e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 1.168569e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.55-269G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-269G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+300G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+102G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+102G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4750
bin: 1.75e1
variant carriers: 61

GenotypeDepth
all individuals: 15953
bin: 2.75e1
variant carriers: 50

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6746
bin: 7.5e0
variant carriers: 19

GenotypeDepth
all individuals: 516
bin: 4.25e1
variant carriers: 7

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13867
bin: 1.25e1
variant carriers: 41

GenotypeDepth
all individuals: 37
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1291
bin: 3.75e1
variant carriers: 16

GenotypeDepth
all individuals: 4412
bin: 2.5e0
variant carriers: 5

GenotypeDepth
all individuals: 6010
bin: 3.25e1
variant carriers: 28

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 6

GenotypeDepth
all individuals: 122
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6286
bin: 2.25e1
variant carriers: 63

GenotypeQuality
all individuals: 20606
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 368
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4089
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 825
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 13291
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1201
bin: 9.75e1
variant carriers: 273

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4520
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2070
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1227
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 542
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 441
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 1

Latino
type: Population
allele count: 14
allele frequency: 1.434132349928293e-3
allele num: 9762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.656089527924355e-4
allele num: 56474
num of homozygotes: 0

South Asian
type: Population
allele count: 86
allele frequency: 9.628302731751007e-3
allele num: 8932
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

African
type: Population
allele count: 165
allele frequency: 1.875426233234826e-2
allele num: 8798
num of homozygotes: 2

Other
type: Population
allele count: 1
allele frequency: 1.400560224089636e-3
allele num: 714
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.168569e6

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

QD
type: SiteQuality
SIO_000300: 1.265e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+305dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+107dupC
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+107dupC
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 1245
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5658
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4601
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6007
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14566
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15058
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6840
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 5352
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 507
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4790
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13628
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.213e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 1.144172e6

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+303C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-266C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+105C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+105C>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 15176
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5563
bin: 2.25e1
variant carriers: 17

GenotypeDepth
all individuals: 6365
bin: 1.75e1
variant carriers: 6

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1221
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13897
bin: 2.75e1
variant carriers: 10

GenotypeDepth
all individuals: 6904
bin: 7.5e0
variant carriers: 5

GenotypeDepth
all individuals: 4750
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5415
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2765
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4945
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5061
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13535
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1012
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3889
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17674
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 6.229235880398671e-4
allele num: 9632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

East Asian
type: Population
allele count: 34
allele frequency: 4.868270332187858e-3
allele num: 6984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.063e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.144e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

DP
type: SiteQuality
SIO_000300: 1.119543e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+306T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+108T>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+108T>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4952
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15892
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8090
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4877
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12290
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4939
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7007
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 500
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5187
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 299
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15619
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.147578609134726e-4
allele num: 8714
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

DP
type: SiteQuality
SIO_000300: 1.083512e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

QD
type: SiteQuality
SIO_000300: 3.55e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-262C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+109C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+109C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16015
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1144
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10843
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5098
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4593
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7226
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9845
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4433
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 929
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4462
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4205
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5342
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13157
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6370
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.099512266142535e-5
allele num: 54948
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6826
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

QD
type: SiteQuality
SIO_000300: 1.342e1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.05258e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.55-260C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-260C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+309C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+111C>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-260C>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16007
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10388
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10409
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4165
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5193
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7373
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4550
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5399
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12905
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.304601899196493e-5
allele num: 54760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.039994e6

QD
type: SiteQuality
SIO_000300: 1.07e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 6.393e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.604e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.186+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-258C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+311C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-258C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+113C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5265
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3804
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15909
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7637
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1092
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4352
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11854
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9247
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6835
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5500
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4957
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.489425081918379e-4
allele num: 6714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.018125e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.225e0

QD
type: SiteQuality
SIO_000300: 6.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

VQSLOD
type: SiteQuality
SIO_000300: -1.133e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+317C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.252+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432850
ensembl transcript: ENST00000528163
gene symbol: IL32
hgvsc: ENST00000528163.2:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+119C>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449483
ensembl transcript: ENST00000548476
gene symbol: IL32
hgvsc: ENST00000548476.1:c.252+119C>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 486
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15203
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5489
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5366
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2923
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1026
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8594
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6647
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13851
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5896
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5693
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 836
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12042
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.884729918202722e-5
allele num: 53058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 9.73742e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 2.895e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.84+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+318G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+120G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+120G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5366
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13708
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9103
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5637
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2672
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1016
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14830
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6734
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4743
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5671
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11195
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.634170547370028e-5
allele num: 52396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.284026707755521e-4
allele num: 7788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.258e0

FS
type: SiteQuality
SIO_000300: 5.352e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.966e-1

DP
type: SiteQuality
SIO_000300: 9.61282e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-247G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.252+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.252+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.114+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.114+124G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-247G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+124G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2232
bin: 3.25e1
variant carriers: 12

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8313
bin: 2.25e1
variant carriers: 62

GenotypeDepth
all individuals: 4487
bin: 2.75e1
variant carriers: 35

GenotypeDepth
all individuals: 983
bin: 3.75e1
variant carriers: 8

GenotypeDepth
all individuals: 119
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 5374
bin: 2.5e0
variant carriers: 6

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9942
bin: 7.5e0
variant carriers: 67

GenotypeDepth
all individuals: 485
bin: 4.25e1
variant carriers: 6

GenotypeDepth
all individuals: 13408
bin: 1.75e1
variant carriers: 100

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14294
bin: 1.25e1
variant carriers: 112

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6136
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 598
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3041
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 296
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 670
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 7227
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2483
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1242
bin: 9.75e1
variant carriers: 333

GenotypeQuality
all individuals: 1116
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1628
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2702
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 8871
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4560
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4561
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5378
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3063
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 879
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3972
bin: 4.75e1
variant carriers: 1

Latino
type: Population
allele count: 23
allele frequency: 2.894538132393657e-3
allele num: 7946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.966522549680695e-5
allele num: 50422
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.651800462504129e-4
allele num: 6054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5778
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.754693366708385e-4
allele num: 7990
num of homozygotes: 0

African
type: Population
allele count: 321
allele frequency: 4.343707713125846e-2
allele num: 7390
num of homozygotes: 8

Other
type: Population
allele count: 1
allele frequency: 1.54320987654321e-3
allele num: 648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.403e1

VQSLOD
type: SiteQuality
SIO_000300: 4.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.977e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.45152e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.54+323C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-246C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.252+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.114+125C>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.252+125C>G
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14359
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9966
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2178
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8355
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5387
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13320
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4302
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3043
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5405
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3993
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7358
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.341561577676415e-4
allele num: 7454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

QD
type: SiteQuality
SIO_000300: 1.329e1

MQ
type: SiteQuality
SIO_000300: 5.863e1

VQSLOD
type: SiteQuality
SIO_000300: -2.457e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 1.5315e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.588e0

DP
type: SiteQuality
SIO_000300: 9.4402e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.395e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432917
ensembl transcript: ENST00000533097
gene symbol: IL32
hgvsc: ENST00000533097.2:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.115-245G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.115-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-49G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.253-49G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 3351
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1121
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8195
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7546
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6448
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1405
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8222
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3631
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6009
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2497
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3467
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4571
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36473
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3354
bin: 7.75e1
variant carriers: 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: 66564
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

DP
type: SiteQuality
SIO_000300: 2.904221e6

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.358e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.115-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.115-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.115-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.115-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.85-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.253-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.187-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.115-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-49G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.55-245G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1661
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7546
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8222
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6448
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3631
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1405
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6009
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1121
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3351
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8195
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3467
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4571
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36473
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.904221e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.253-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.253-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.115-48G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.253-48G>A
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 6219
bin: 2.75e1
variant carriers: 4712

GenotypeDepth
all individuals: 877
bin: 7.75e1
variant carriers: 799

GenotypeDepth
all individuals: 4749
bin: 5.25e1
variant carriers: 4200

GenotypeDepth
all individuals: 406
bin: 8.75e1
variant carriers: 357

GenotypeDepth
all individuals: 6062
bin: 4.75e1
variant carriers: 5215

GenotypeDepth
all individuals: 84
bin: 7.5e0
variant carriers: 66

GenotypeDepth
all individuals: 1806
bin: 6.75e1
variant carriers: 1633

GenotypeDepth
all individuals: 2597
bin: 6.25e1
variant carriers: 2326

GenotypeDepth
all individuals: 3441
bin: 2.25e1
variant carriers: 2739

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 3217

GenotypeDepth
all individuals: 632
bin: 8.25e1
variant carriers: 576

GenotypeDepth
all individuals: 8226
bin: 3.75e1
variant carriers: 6756

GenotypeDepth
all individuals: 1381
bin: 1.75e1
variant carriers: 1186

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 3

GenotypeDepth
all individuals: 7422
bin: 4.25e1
variant carriers: 6204

GenotypeDepth
all individuals: 315
bin: 9.25e1
variant carriers: 270

GenotypeDepth
all individuals: 434
bin: 1.25e1
variant carriers: 358

GenotypeDepth
all individuals: 3385
bin: 9.75e1
variant carriers: 3051

GenotypeDepth
all individuals: 1226
bin: 7.25e1
variant carriers: 1092

GenotypeDepth
all individuals: 7842
bin: 3.25e1
variant carriers: 6148

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 58

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 28

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 50

GenotypeQuality
all individuals: 490
bin: 5.25e1
variant carriers: 331

GenotypeQuality
all individuals: 48308
bin: 9.75e1
variant carriers: 44667

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 56

GenotypeQuality
all individuals: 884
bin: 8.75e1
variant carriers: 524

GenotypeQuality
all individuals: 1504
bin: 6.75e1
variant carriers: 590

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 987

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 148

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 24

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 34

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 128

GenotypeQuality
all individuals: 380
bin: 5.75e1
variant carriers: 288

GenotypeQuality
all individuals: 1920
bin: 6.25e1
variant carriers: 505

GenotypeQuality
all individuals: 914
bin: 7.25e1
variant carriers: 408

GenotypeQuality
all individuals: 392
bin: 4.75e1
variant carriers: 242

GenotypeQuality
all individuals: 1582
bin: 7.75e1
variant carriers: 841

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 109

GenotypeQuality
all individuals: 1565
bin: 8.25e1
variant carriers: 890

Other
type: Population
allele count: 558
allele frequency: 6.172566371681416e-1
allele num: 904
num of homozygotes: 179

Latino
type: Population
allele count: 5261
allele frequency: 4.587547959539588e-1
allele num: 11468
num of homozygotes: 1226

African
type: Population
allele count: 6095
allele frequency: 5.886613869036121e-1
allele num: 10354
num of homozygotes: 1810

European (Non-Finnish)
type: Population
allele count: 43689
allele frequency: 6.583436303908864e-1
allele num: 66362
num of homozygotes: 14350

South Asian
type: Population
allele count: 9356
allele frequency: 5.675806842999273e-1
allele num: 16484
num of homozygotes: 2670

East Asian
type: Population
allele count: 3991
allele frequency: 4.653684701492538e-1
allele num: 8576
num of homozygotes: 930

European (Finnish)
type: Population
allele count: 4406
allele frequency: 6.745254133496632e-1
allele num: 6532
num of homozygotes: 1479

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

QD
type: SiteQuality
SIO_000300: 2.284e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

DP
type: SiteQuality
SIO_000300: 2.932215e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.115-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.115-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000371648
ensembl transcript: ENST00000382213
gene symbol: IL32
hgvsc: ENST00000382213.3:c.115-243G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.115-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.253-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-47G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.55-243G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 1180
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4110
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1346
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9414
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10326
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1774
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7080
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8709
bin: 3.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 5105
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3745
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2551
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8662
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25261
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004807692307692e-5
allele num: 66560
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.259e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 1.0537e1

DP
type: SiteQuality
SIO_000300: 2.596744e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0

VQSLOD
type: SiteQuality
SIO_000300: -1.152e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.85-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.115-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000008180
ensembl transcript: ENST00000008180
gene symbol: IL32
hgvsc: ENST00000008180.9:c.55-47G>T
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.115-243G>T
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 7080
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5105
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10326
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9414
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1180
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3745
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8709
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4110
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1346
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 571
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8662
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25261
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4385
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502403846153846e-5
allele num: 66560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.152e0

QD
type: SiteQuality
SIO_000300: 1.259e1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 1.0537e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0

DP
type: SiteQuality
SIO_000300: 2.596744e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000405063
ensembl transcript: ENST00000440815
gene symbol: IL32
hgvsc: ENST00000440815.3:c.115-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447033
ensembl transcript: ENST00000552936
gene symbol: IL32
hgvsc: ENST00000552936.1:c.187-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.115-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.55-238G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.115-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.115-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.115-238G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.253-42G>C
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-42G>C
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 8711
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3743
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9544
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10347
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1181
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 965
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5107
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7072
bin: 4.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1773
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4353
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2549
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25234
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4320
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4587
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5575
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.59895e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.674e0

QD
type: SiteQuality
SIO_000300: 2.568e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447979
ensembl transcript: ENST00000548246
gene symbol: IL32
hgvsc: ENST00000548246.1:c.55-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433866
ensembl transcript: ENST00000525377
gene symbol: IL32
hgvsc: ENST00000525377.2:c.253-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.115-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447496
ensembl transcript: ENST00000551122
gene symbol: IL32
hgvsc: ENST00000551122.1:c.115-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431740
ensembl transcript: ENST00000525228
gene symbol: IL32
hgvsc: ENST00000525228.1:c.55-237A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.55-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.115-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000432218
ensembl transcript: ENST00000525643
gene symbol: IL32
hgvsc: ENST00000525643.2:c.115-41A>G
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000324742
ensembl transcript: ENST00000325568
gene symbol: IL32
hgvsc: ENST00000325568.5:c.115-41A>G
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5108
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9580
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4433
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 10350
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8699
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3741
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2549
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1774
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7072
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5597
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25233
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.033e1

FS
type: SiteQuality
SIO_000300: 3.811e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 2.599567e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.279e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.253-235delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000411958
ensembl transcript: ENST00000444393
gene symbol: IL32
hgvsc: ENST00000444393.3:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446978
ensembl transcript: ENST00000552356
gene symbol: IL32
hgvsc: ENST00000552356.1:c.55-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433747
ensembl transcript: ENST00000530890
gene symbol: IL32
hgvsc: ENST00000530890.1:c.55-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000450364
ensembl transcript: ENST00000526464
gene symbol: IL32
hgvsc: ENST00000526464.2:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436937
ensembl transcript: ENST00000529699
gene symbol: IL32
hgvsc: ENST00000529699.1:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380096
ensembl transcript: ENST00000396887
gene symbol: IL32
hgvsc: ENST00000396887.3:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-39delG
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000433177
ensembl transcript: ENST00000531965
gene symbol: IL32
hgvsc: ENST00000531965.1:c.85-39delG
variant of: http://identifiers.org/hgnc/16830

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10350
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2549
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5108
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8699
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9580
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4433
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7072
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1774
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3741
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25233
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 10047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5597
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.599567e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.279e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.811e0

QD
type: SiteQuality
SIO_000300: 1.033e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000008517
ensembl transcript: ENST00000532247
gene symbol: IL32
hgvsc: ENST00000532247.1:n.660G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448354
ensembl transcript: ENST00000548807
gene symbol: IL32
hgvsc: ENST00000548807.1:c.253-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000449147
ensembl transcript: ENST00000551513
gene symbol: IL32
hgvsc: ENST00000551513.1:c.253-236G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000448683
ensembl transcript: ENST00000552664
gene symbol: IL32
hgvsc: ENST00000552664.1:c.115-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000437020
ensembl transcript: ENST00000529550
gene symbol: IL32
hgvsc: ENST00000529550.1:c.115-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000380099
ensembl transcript: ENST00000396890
gene symbol: IL32
hgvsc: ENST00000396890.2:c.253-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000431775
ensembl transcript: ENST00000534507
gene symbol: IL32
hgvsc: ENST00000534507.1:c.253-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000447812
ensembl transcript: ENST00000549213
gene symbol: IL32
hgvsc: ENST00000549213.1:c.115-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000436929
ensembl transcript: ENST00000530538
gene symbol: IL32
hgvsc: ENST00000530538.2:c.115-40G>A
variant of: http://identifiers.org/hgnc/16830

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000008517
ensembl protein: ENSP00000446624
ensembl transcript: ENST00000548652
gene symbol: IL32
hgvsc: ENST00000548652.1:c.115-236G>A
variant of: http://identifiers.org/hgnc/16830

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

GenotypeDepth
all individuals: 5108
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1181
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 805
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3741
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8701
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2363
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 838
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2550
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10369
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4461
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9585
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1773
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variant carriers: 0

GenotypeDepth
all individuals: 274
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variant carriers: 0

GenotypeDepth
all individuals: 7074
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
all individuals: 2370
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variant carriers: 0

GenotypeQuality
all individuals: 5590
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variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10045
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 229
bin: 2.25e1
variant carriers: 0

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