9-34657070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657070
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657070
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.370G>A
  hgvsp: ENSP00000451447.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.370G>A
  hgvsp: ENSP00000450640.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.370G>A
  hgvsp: ENSP00000450543.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.370G>A
  hgvsp: ENSP00000450565.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.370G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.200G>A
  hgvsp: ENSP00000451553.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.370G>A
  hgvsp: ENSP00000326500.8:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258728
  ensembl protein: ENSP00000451792
  ensembl transcript: ENST00000556278
  gene symbol: GALT
  hgvsc: ENST00000556278.1:c.802G>A
  hgvsp: ENSP00000451792.1:p.Asp268Asn
  variant of: http://identifiers.org/hgnc/4135
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.139G>A
  hgvsp: ENSP00000452207.1:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.370G>A
  hgvsp: ENSP00000394391.2:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.370G>A
  hgvsp: ENSP00000473647.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.370G>A
  hgvsp: ENSP00000368094.3:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp268Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

9-34657075-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657075
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657075
    reference: chr 9
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.375T>C
  hgvsp: ENST00000602473.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.375T>C
  hgvsp: ENST00000318041.9:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.375T>C
  hgvsp: ENST00000378817.4:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.375T>C
  hgvsp: ENST00000556531.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.205T>C
  hgvsp: ENSP00000451553.1:p.Ter69ArgextTer31
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.375T>C
  hgvsp: ENST00000555003.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.375T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.375T>C
  hgvsp: ENST00000441545.2:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.375T>C
  hgvsp: ENST00000555981.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000258728
  ensembl protein: ENSP00000451792
  ensembl transcript: ENST00000556278
  gene symbol: GALT
  hgvsc: ENST00000556278.1:c.807T>C
  hgvsp: ENST00000556278.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4135
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.144T>C
  hgvsp: ENST00000553620.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*149T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.375T>C
  hgvsp: ENST00000556792.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter69ArgextTer31
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

9-34657077-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657077
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657077
    reference: chr 9
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.377A>G
  hgvsp: ENSP00000394391.2:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.377A>G
  hgvsp: ENSP00000368094.3:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.207A>G
  hgvsp: ENSP00000451553.1:p.Ter69TrpextTer31
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.377A>G
  hgvsp: ENSP00000451447.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.377A>G
  hgvsp: ENSP00000326500.8:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.377A>G
  hgvsp: ENSP00000473647.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.377A>G
  hgvsp: ENSP00000450640.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.146A>G
  hgvsp: ENSP00000452207.1:p.Glu49Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.377A>G
  hgvsp: ENSP00000450543.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*151A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.377A>G
  hgvsp: ENSP00000450565.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.377A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258728
  ensembl protein: ENSP00000451792
  ensembl transcript: ENST00000556278
  gene symbol: GALT
  hgvsc: ENST00000556278.1:c.809A>G
  hgvsp: ENSP00000451792.1:p.Glu270Gly
  variant of: http://identifiers.org/hgnc/4135
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter69TrpextTer31
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

9-34657108-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657108
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657108
    reference: chr 9
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*182G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000258728
  ensembl protein: ENSP00000451792
  ensembl transcript: ENST00000556278
  gene symbol: GALT
  hgvsc: ENST00000556278.1:c.840G>T
  hgvsp: ENSP00000451792.1:p.Gln280His
  variant of: http://identifiers.org/hgnc/4135
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.408G>T
  hgvsp: ENSP00000368094.3:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.408G>T
  hgvsp: ENSP00000450565.1:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.408G>T
  hgvsp: ENSP00000326500.8:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.408G>T
  hgvsp: ENSP00000394391.2:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.408G>T
  hgvsp: ENSP00000450640.1:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.408G>T
  hgvsp: ENSP00000473647.1:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.177G>T
  hgvsp: ENSP00000452207.1:p.Gln59His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.408G>T
  hgvsp: ENSP00000450543.1:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.408G>T
  hgvsp: ENSP00000451447.1:p.Gln136His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*31G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.408G>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln280His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

9-34657112-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657112
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657112
    reference: chr 9
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.181A>T
  hgvsp: ENSP00000452207.1:p.Ser61Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.412A>T
  hgvsp: ENSP00000450543.1:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.412A>T
  hgvsp: ENSP00000394391.2:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.412A>T
  hgvsp: ENSP00000473647.1:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.412A>T
  hgvsp: ENSP00000450565.1:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*35A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.412A>T
  hgvsp: ENSP00000451447.1:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.412A>T
  hgvsp: ENSP00000368094.3:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.412A>T
  hgvsp: ENSP00000326500.8:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.412A>T
  hgvsp: ENSP00000450640.1:p.Ser138Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*186A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.412A>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser138Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

9-34657114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657114
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657114
    reference: chr 9
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*188C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.414C>T
  hgvsp: ENST00000556792.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.414C>T
  hgvsp: ENST00000318041.9:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.414C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.414C>T
  hgvsp: ENST00000602473.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.414C>T
  hgvsp: ENST00000441545.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.414C>T
  hgvsp: ENST00000555003.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.414C>T
  hgvsp: ENST00000556531.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.414C>T
  hgvsp: ENST00000378817.4:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.414C>T
  hgvsp: ENST00000555981.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.183C>T
  hgvsp: ENST00000553620.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: n.414C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-34657115-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657115
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657115
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.415G>C
  hgvsp: ENSP00000450543.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.415G>C
  hgvsp: ENSP00000450640.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.184G>C
  hgvsp: ENSP00000452207.1:p.Gly62Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.415G>C
  hgvsp: ENSP00000394391.2:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.415G>C
  hgvsp: ENSP00000450565.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.415G>C
  hgvsp: ENSP00000326500.8:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.415G>C
  hgvsp: ENSP00000368094.3:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*38G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.415G>C
  hgvsp: ENSP00000473647.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*189G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.415G>C
  hgvsp: ENSP00000451447.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly139Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS

9-34657116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657116
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657116
    reference: chr 9
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.416G>A
  hgvsp: ENSP00000326500.8:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450543
  ensembl transcript: ENST00000556792
  gene symbol: IL11RA
  hgvsc: ENST00000556792.1:c.416G>A
  hgvsp: ENSP00000450543.1:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.185G>A
  hgvsp: ENSP00000452207.1:p.Gly62Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.416G>A
  hgvsp: ENSP00000368094.3:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.416G>A
  hgvsp: ENSP00000394391.2:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.416G>A
  hgvsp: ENSP00000450565.1:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.416G>A
  hgvsp: ENSP00000473647.1:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.416G>A
  hgvsp: ENSP00000451447.1:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*190G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.416G>A
  hgvsp: ENSP00000450640.1:p.Gly139Asp
  variant of: http://identifiers.org/hgnc/5967
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.415+1G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

9-34657127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657127
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657127
    reference: chr 9
allele count: 19
allele frequency: 1.564996787638173e-4
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.427C>T
  hgvsp: ENSP00000326500.8:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.427C>T
  hgvsp: ENSP00000394391.2:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.427C>T
  hgvsp: ENSP00000451447.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.427C>T
  hgvsp: ENSP00000473647.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.427C>T
  hgvsp: ENSP00000450565.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.427C>T
  hgvsp: ENSP00000450640.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*201C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.196C>T
  hgvsp: ENSP00000452207.1:p.Arg66Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.427C>T
  hgvsp: ENSP00000368094.3:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+12C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg143Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

9-34657128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657128
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657128
    reference: chr 9
allele count: 9
allele frequency: 7.413020558777017e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.428G>A
  hgvsp: ENSP00000450565.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.428G>A
  hgvsp: ENSP00000451447.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.428G>A
  hgvsp: ENSP00000450640.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.428G>A
  hgvsp: ENSP00000473647.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.428G>A
  hgvsp: ENSP00000368094.3:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*202G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.197G>A
  hgvsp: ENSP00000452207.1:p.Arg66His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.428G>A
  hgvsp: ENSP00000394391.2:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+13G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*51G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.428G>A
  hgvsp: ENSP00000326500.8:p.Arg143His
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg143His
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: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

9-34657130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657130
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657130
    reference: chr 9
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.430T>G
  hgvsp: ENSP00000368094.3:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.430T>G
  hgvsp: ENSP00000451447.1:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.430T>G
  hgvsp: ENSP00000473647.1:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*204T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*53T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.430T>G
  hgvsp: ENSP00000394391.2:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.430T>G
  hgvsp: ENSP00000326500.8:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+15T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.199T>G
  hgvsp: ENSP00000452207.1:p.Tyr67Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.430T>G
  hgvsp: ENSP00000450640.1:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.430T>G
  hgvsp: ENSP00000450565.1:p.Tyr144Asp
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr144Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-34657131-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657131
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657131
    reference: chr 9
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.431A>C
  hgvsp: ENSP00000450640.1:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.431A>C
  hgvsp: ENSP00000451447.1:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+16A>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.431A>C
  hgvsp: ENSP00000368094.3:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.431A>C
  hgvsp: ENSP00000394391.2:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.431A>C
  hgvsp: ENSP00000450565.1:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*205A>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.200A>C
  hgvsp: ENSP00000452207.1:p.Tyr67Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*54A>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.431A>C
  hgvsp: ENSP00000326500.8:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.431A>C
  hgvsp: ENSP00000473647.1:p.Tyr144Ser
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr144Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-34657136-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657136
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657136
    reference: chr 9
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.436A>C
  hgvsp: ENSP00000394391.2:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.436A>C
  hgvsp: ENSP00000473647.1:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.436A>C
  hgvsp: ENSP00000450565.1:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+21A>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.436A>C
  hgvsp: ENSP00000451447.1:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.436A>C
  hgvsp: ENSP00000326500.8:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*210A>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.436A>C
  hgvsp: ENSP00000450640.1:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.205A>C
  hgvsp: ENSP00000452207.1:p.Thr69Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.436A>C
  hgvsp: ENSP00000368094.3:p.Thr146Pro
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*59A>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr146Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-34657147-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657147
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657147
    reference: chr 9
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+32G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+1G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+1G>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: c.446+1G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

9-34657148-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657148
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657148
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+2T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+33T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+2T>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7365
  bin: 6.25e1
  variant carriers: 0
hgvs: c.446+2T>C
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-34657149-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657149
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657149
    reference: chr 9
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+34G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+3G>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.446+3G>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/9-34657176-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657176
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657176
    reference: chr 9
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+61C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+30C>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

9-34657185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657185
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657185
    reference: chr 9
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+70G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+39G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+39G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-34657189-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657189
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657189
    reference: chr 9
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+74G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+43G>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-34657196-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657196
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657196
    reference: chr 9
allele count: 3
allele frequency: 2.473451619286327e-5
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+81C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+50C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+50C>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4216
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

9-34657198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657198
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657198
    reference: chr 9
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.415+83A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*69+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*220+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.215+52A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.446+52A>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

9-34657241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657241
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657241
    reference: chr 9
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-70C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447-59C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

9-34657256-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657256
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657256
    reference: chr 9
allele count: 2
allele frequency: 1.652046059044126e-5
allele num: 121062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-55G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447-44G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

9-34657268-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657268
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657268
    reference: chr 9
allele count: 2
allele frequency: 1.650083329208125e-5
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-43T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70-32T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447-32T>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

9-34657272-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657272
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657272
    reference: chr 9
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-39T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70-28T>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447-28T>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

9-34657283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657283
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657283
    reference: chr 9
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-28G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447-17G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

9-34657300-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657300
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657300
    reference: chr 9
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.447G>T
  hgvsp: ENSP00000450565.1:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.447G>T
  hgvsp: ENSP00000473647.1:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.447G>T
  hgvsp: ENSP00000394391.2:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.447G>T
  hgvsp: ENSP00000326500.8:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*70G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*221G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.447G>T
  hgvsp: ENSP00000450640.1:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.216G>T
  hgvsp: ENSP00000452207.1:p.Arg72Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.447G>T
  hgvsp: ENSP00000368094.3:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-11G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.447G>T
  hgvsp: ENSP00000451447.1:p.Arg149Ser
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg149Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

9-34657307-A-ACAGTCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657307
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657314
    reference: chr 9
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: ACAGTCCC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.418_419insCCAGTCC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.460_461insCCAGTCC
  hgvsp: ENSP00000451447.1:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.460_461insCCAGTCC
  hgvsp: ENSP00000394391.2:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.460_461insCCAGTCC
  hgvsp: ENSP00000473647.1:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.229_230insCCAGTCC
  hgvsp: ENSP00000452207.1:p.Leu77ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*234_*235insCCAGTCC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*83_*84insCCAGTCC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.460_461insCCAGTCC
  hgvsp: ENSP00000450565.1:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.460_461insCCAGTCC
  hgvsp: ENSP00000450640.1:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.460_461insCCAGTCC
  hgvsp: ENSP00000368094.3:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.460_461insCCAGTCC
  hgvsp: ENSP00000326500.8:p.Leu154ProfsTer6
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu154ProfsTer6
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

9-34657308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657308
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657308
    reference: chr 9
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.224C>T
  hgvsp: ENSP00000452207.1:p.Thr75Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*78C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.455C>T
  hgvsp: ENSP00000451447.1:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.455C>T
  hgvsp: ENSP00000450565.1:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.455C>T
  hgvsp: ENSP00000326500.8:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.455C>T
  hgvsp: ENSP00000394391.2:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.455C>T
  hgvsp: ENSP00000450640.1:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.455C>T
  hgvsp: ENSP00000473647.1:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.455C>T
  hgvsp: ENSP00000368094.3:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-3C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr152Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-34657309-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657309
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657309
    reference: chr 9
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.456A>T
  hgvsp: ENST00000555003.1:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.416-2A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.456A>T
  hgvsp: ENST00000441545.2:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.225A>T
  hgvsp: ENST00000553620.1:c.225A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.456A>T
  hgvsp: ENST00000556531.1:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.456A>T
  hgvsp: ENST00000378817.4:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.456A>T
  hgvsp: ENST00000555981.1:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*230A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*79A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.456A>T
  hgvsp: ENST00000318041.9:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.456A>T
  hgvsp: ENST00000602473.1:c.456A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
canonical: false
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.416-2A>T
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-34657320-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657320
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657320
    reference: chr 9
allele count: 18
allele frequency: 1.482921685258111e-4
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.467C>G
  hgvsp: ENSP00000368094.3:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.467C>G
  hgvsp: ENSP00000450565.1:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.467C>G
  hgvsp: ENSP00000326500.8:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.467C>G
  hgvsp: ENSP00000450640.1:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.236C>G
  hgvsp: ENSP00000452207.1:p.Ala79Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.467C>G
  hgvsp: ENSP00000451447.1:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.467C>G
  hgvsp: ENSP00000473647.1:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.467C>G
  hgvsp: ENSP00000394391.2:p.Ala156Gly
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*241C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.425C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*90C>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala156Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

9-34657324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657324
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657324
    reference: chr 9
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.240T>C
  hgvsp: ENST00000553620.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*94T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.471T>C
  hgvsp: ENST00000441545.2:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.471T>C
  hgvsp: ENST00000378817.4:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.471T>C
  hgvsp: ENST00000556531.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*245T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.471T>C
  hgvsp: ENST00000602473.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.471T>C
  hgvsp: ENST00000318041.9:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.471T>C
  hgvsp: ENST00000555003.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.471T>C
  hgvsp: ENST00000555981.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.429T>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp157Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-34657332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657332
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657332
    reference: chr 9
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479G>A
  hgvsp: ENSP00000450640.1:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479G>A
  hgvsp: ENSP00000326500.8:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479G>A
  hgvsp: ENSP00000451447.1:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479G>A
  hgvsp: ENSP00000450565.1:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479G>A
  hgvsp: ENSP00000473647.1:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479G>A
  hgvsp: ENSP00000394391.2:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479G>A
  hgvsp: ENSP00000368094.3:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248G>A
  hgvsp: ENSP00000452207.1:p.Arg83Lys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg160Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

9-34657333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657333
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657333
    reference: chr 9
allele count: 9
allele frequency: 7.414730598121601e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+1G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 7.75e1
  variant carriers: 0
hgvs: c.479+1G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

9-34657339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657339
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657339
    reference: chr 9
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+7C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14050
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.479+7C>T
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

9-34657340-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657340
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657340
    reference: chr 9
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+8G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+8G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.479+8G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-34657352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657352
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657352
    reference: chr 9
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+20G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+20G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
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: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

9-34657353-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657353
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657353
    reference: chr 9
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+21T>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40598
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-34657357-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657357
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657357
    reference: chr 9
allele count: 3
allele frequency: 2.471658317954126e-5
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+25G>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40559
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/9-34657361-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657361
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657361
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+29C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+29C>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-34657361-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657361
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657361
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+29C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+29C>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

9-34657365-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657365
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657365
    reference: chr 9
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+33C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+33C>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

9-34657365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657365
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657365
    reference: chr 9
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+33C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

9-34657368-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657368
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657368
    reference: chr 9
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+36G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+36G>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-34657369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657369
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657369
    reference: chr 9
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+37G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

9-34657373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657373
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657373
    reference: chr 9
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+41C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+41C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

9-34657375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657375
    reference: chr 9
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.437+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*253+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.248+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*102+43C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.479+43C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

9-34657378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657378
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657378
    reference: chr 9
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-40T>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-40T>C
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-34657383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657383
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657383
    reference: chr 9
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-35A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-35A>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

9-34657390-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657390
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657390
    reference: chr 9
allele count: 839
allele frequency: 6.912973979532983e-3
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-28A>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27521
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 13888
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 45
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-34657395-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657395
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657395
    reference: chr 9
allele count: 720
allele frequency: 5.932664260641716e-3
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-23A>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13984
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 27739
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 21
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-34657406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657406
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657406
    reference: chr 9
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-12C>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-34657407-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657407
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657407
    reference: chr 9
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.438-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*254-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*103-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.249-11C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.480-11C>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-34657423-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657423
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657423
    reference: chr 9
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.485G>A
  hgvsp: ENSP00000451447.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.485G>A
  hgvsp: ENSP00000368094.3:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.485G>A
  hgvsp: ENSP00000326500.8:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.485G>A
  hgvsp: ENSP00000450640.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.485G>A
  hgvsp: ENSP00000473647.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*259G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.254G>A
  hgvsp: ENSP00000452207.1:p.Ser85Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*108G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.485G>A
  hgvsp: ENSP00000450565.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.485G>A
  hgvsp: ENSP00000394391.2:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.443G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser162Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

9-34657425-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657425
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657425
    reference: chr 9
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.487C>G
  hgvsp: ENSP00000451447.1:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.487C>G
  hgvsp: ENSP00000473647.1:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.256C>G
  hgvsp: ENSP00000452207.1:p.Pro86Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.487C>G
  hgvsp: ENSP00000450640.1:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.487C>G
  hgvsp: ENSP00000368094.3:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.487C>G
  hgvsp: ENSP00000326500.8:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*261C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.487C>G
  hgvsp: ENSP00000394391.2:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.487C>G
  hgvsp: ENSP00000450565.1:p.Pro163Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.445C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*110C>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro163Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

9-34657436-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657436
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657436
    reference: chr 9
allele count: 15
allele frequency: 1.236501525018548e-4
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.498G>C
  hgvsp: ENST00000441545.2:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.498G>C
  hgvsp: ENST00000318041.9:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.498G>C
  hgvsp: ENST00000602473.1:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.456G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.498G>C
  hgvsp: ENST00000555003.1:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*121G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*272G>C
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.498G>C
  hgvsp: ENST00000555981.1:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.267G>C
  hgvsp: ENST00000553620.1:c.267G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451447
  ensembl transcript: ENST00000556531
  gene symbol: IL11RA
  hgvsc: ENST00000556531.1:c.498G>C
  hgvsp: ENST00000556531.1:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.498G>C
  hgvsp: ENST00000378817.4:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28045
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly166Gly
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-34657443-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657443
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657443
    reference: chr 9
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*128C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.505C>G
  hgvsp: ENSP00000368094.3:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.505C>G
  hgvsp: ENSP00000450640.1:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.505C>G
  hgvsp: ENSP00000473647.1:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.274C>G
  hgvsp: ENSP00000452207.1:p.Pro92Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.505C>G
  hgvsp: ENSP00000394391.2:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.505C>G
  hgvsp: ENSP00000450565.1:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.505C>G
  hgvsp: ENSP00000326500.8:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.463C>G
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*279C>G
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro169Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-34657456-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657456
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657456
    reference: chr 9
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.518A>T
  hgvsp: ENSP00000326500.8:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*292A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.287A>T
  hgvsp: ENSP00000452207.1:p.Asp96Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.476A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.518A>T
  hgvsp: ENSP00000394391.2:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.518A>T
  hgvsp: ENSP00000450565.1:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.518A>T
  hgvsp: ENSP00000450640.1:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*141A>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.518A>T
  hgvsp: ENSP00000473647.1:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.518A>T
  hgvsp: ENSP00000368094.3:p.Asp173Val
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28040
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp173Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

9-34657459-CCCTAGGGGCTGCCCGCTGTGTTGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657459
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657435
    reference: chr 9
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsp: ENSP00000394391.2:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsp: ENSP00000452207.1:p.Leu98_Val105del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsp: ENSP00000368094.3:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsp: ENSP00000326500.8:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsp: ENSP00000450640.1:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsp: ENSP00000450565.1:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsp: ENSP00000473647.1:p.Leu175_Val182del
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu175_Val182del
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: CCCTAGGGGCTGCCCGCTGTGTTGT
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

9-34657464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657464
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657464
    reference: chr 9
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*300G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.526G>A
  hgvsp: ENSP00000473647.1:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.526G>A
  hgvsp: ENSP00000368094.3:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.526G>A
  hgvsp: ENSP00000450640.1:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.295G>A
  hgvsp: ENSP00000452207.1:p.Gly99Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.484G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.526G>A
  hgvsp: ENSP00000326500.8:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.526G>A
  hgvsp: ENSP00000394391.2:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.526G>A
  hgvsp: ENSP00000450565.1:p.Gly176Arg
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly176Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

9-34657470-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657470
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657470
    reference: chr 9
allele count: 6
allele frequency: 4.948371985616732e-5
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.532G>T
  hgvsp: ENSP00000450640.1:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.532G>T
  hgvsp: ENSP00000450565.1:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.532G>T
  hgvsp: ENSP00000326500.8:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*155G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.301G>T
  hgvsp: ENSP00000452207.1:p.Ala101Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.532G>T
  hgvsp: ENSP00000394391.2:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*306G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.532G>T
  hgvsp: ENSP00000473647.1:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.532G>T
  hgvsp: ENSP00000368094.3:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.490G>T
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28002
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala178Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-34657471-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657471
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657471
    reference: chr 9
allele count: 3
allele frequency: 2.474022761009401e-5
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.533C>A
  hgvsp: ENSP00000368094.3:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.533C>A
  hgvsp: ENSP00000450640.1:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*156C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.533C>A
  hgvsp: ENSP00000326500.8:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.491C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.533C>A
  hgvsp: ENSP00000450565.1:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.533C>A
  hgvsp: ENSP00000394391.2:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.302C>A
  hgvsp: ENSP00000452207.1:p.Ala101Asp
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*307C>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.533C>A
  hgvsp: ENSP00000473647.1:p.Ala178Asp
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala178Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

9-34657473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657473
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657473
    reference: chr 9
allele count: 80
allele frequency: 6.597938144329897e-4
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.535C>T
  hgvsp: ENSP00000473647.1:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.535C>T
  hgvsp: ENSP00000450640.1:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*309C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.535C>T
  hgvsp: ENSP00000394391.2:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.493C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.535C>T
  hgvsp: ENSP00000368094.3:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.535C>T
  hgvsp: ENSP00000326500.8:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.535C>T
  hgvsp: ENSP00000450565.1:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.304C>T
  hgvsp: ENSP00000452207.1:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28006
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg179Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

9-34657474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657474
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657474
    reference: chr 9
allele count: 8
allele frequency: 6.597829314155642e-5
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.536G>A
  hgvsp: ENSP00000450565.1:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.536G>A
  hgvsp: ENSP00000473647.1:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.494G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.536G>A
  hgvsp: ENSP00000326500.8:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.305G>A
  hgvsp: ENSP00000452207.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.536G>A
  hgvsp: ENSP00000368094.3:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.536G>A
  hgvsp: ENSP00000394391.2:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.536G>A
  hgvsp: ENSP00000450640.1:p.Arg179His
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*310G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*159G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg179His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

9-34657487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657487
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657487
    reference: chr 9
allele count: 9
allele frequency: 7.424762407602956e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.549C>T
  hgvsp: ENST00000555981.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.549C>T
  hgvsp: ENST00000555003.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*323C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.549C>T
  hgvsp: ENST00000441545.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.549C>T
  hgvsp: ENST00000318041.9:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.549C>T
  hgvsp: ENST00000378817.4:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.549C>T
  hgvsp: ENST00000602473.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.507C>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.318C>T
  hgvsp: ENST00000553620.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His183His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-34657488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657488
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657488
    reference: chr 9
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.319G>A
  hgvsp: ENSP00000452207.1:p.Gly107Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.550G>A
  hgvsp: ENSP00000394391.2:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*173G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.550G>A
  hgvsp: ENSP00000450640.1:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.550G>A
  hgvsp: ENSP00000473647.1:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.550G>A
  hgvsp: ENSP00000326500.8:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*324G>A
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.550G>A
  hgvsp: ENSP00000450565.1:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.550G>A
  hgvsp: ENSP00000368094.3:p.Gly184Arg
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.508G>A
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly184Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-34657491-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657491
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657491
    reference: chr 9
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.553G>T
  hgvsp: ENSP00000450565.1:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*327G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.553G>T
  hgvsp: ENSP00000368094.3:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.553G>T
  hgvsp: ENSP00000450640.1:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.511G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.553G>T
  hgvsp: ENSP00000394391.2:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.322G>T
  hgvsp: ENSP00000452207.1:p.Ala108Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.553G>T
  hgvsp: ENSP00000326500.8:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*176G>T
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.553G>T
  hgvsp: ENSP00000473647.1:p.Ala185Ser
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala185Ser
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

9-34657498-TCTGGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34657498
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 34657492
    reference: chr 9
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000394391
  ensembl transcript: ENST00000441545
  gene symbol: IL11RA
  hgvsc: ENST00000441545.2:c.562_567delTGGAGC
  hgvsp: ENSP00000394391.2:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000451553
  ensembl transcript: ENST00000557298
  gene symbol: IL11RA
  hgvsc: ENST00000557298.1:c.*185_*190delTGGAGC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450640
  ensembl transcript: ENST00000555981
  gene symbol: IL11RA
  hgvsc: ENST00000555981.1:c.562_567delTGGAGC
  hgvsp: ENSP00000450640.1:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000326500
  ensembl transcript: ENST00000318041
  gene symbol: IL11RA
  hgvsc: ENST00000318041.9:c.562_567delTGGAGC
  hgvsp: ENSP00000326500.8:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000368094
  ensembl transcript: ENST00000378817
  gene symbol: IL11RA
  hgvsc: ENST00000378817.4:c.562_567delTGGAGC
  hgvsp: ENSP00000368094.3:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450565
  ensembl transcript: ENST00000555003
  gene symbol: IL11RA
  hgvsc: ENST00000555003.1:c.562_567delTGGAGC
  hgvsp: ENSP00000450565.1:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137070
  ensembl transcript: ENST00000478802
  gene symbol: IL11RA
  hgvsc: ENST00000478802.2:n.520_525delTGGAGC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000450707
  ensembl transcript: ENST00000555247
  gene symbol: IL11RA
  hgvsc: ENST00000555247.1:c.*336_*341delTGGAGC
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000473647
  ensembl transcript: ENST00000602473
  gene symbol: IL11RA
  hgvsc: ENST00000602473.1:c.562_567delTGGAGC
  hgvsp: ENSP00000473647.1:p.Trp188_Ser189del
  variant of: http://identifiers.org/hgnc/5967
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137070
  ensembl protein: ENSP00000452207
  ensembl transcript: ENST00000553620
  gene symbol: IL11RA
  hgvsc: ENST00000553620.1:c.331_336delTGGAGC
  hgvsp: ENSP00000452207.1:p.Trp111_Ser112del
  variant of: http://identifiers.org/hgnc/5967
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 28072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Trp188_Ser189del
num of homozygotes: 0
reference allele: TCTGGAG

GenotypeDepth
all individuals: 7943
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 762
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7322
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9159
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7431
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3648
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4056
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3017
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30985
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 4267
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.375e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e0

FS
type: SiteQuality
SIO_000300: 4.711e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

DP
type: SiteQuality
SIO_000300: 2.774393e6

GenotypeDepth
all individuals: 1905
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 896
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3778
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2753
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 10015
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7320
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2664
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7431
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4631
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3017
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30988
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4056
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993766482857828e-5
allele num: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 2.774786e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

GenotypeDepth
all individuals: 742
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9159
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10017
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7320
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1905
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4631
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2664
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3017
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30987
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 4266
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.139e1

FS
type: SiteQuality
SIO_000300: 6.301e0

DP
type: SiteQuality
SIO_000300: 2.774538e6

VQSLOD
type: SiteQuality
SIO_000300: -2.357e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

GenotypeDepth
all individuals: 7941
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1906
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1271
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2698
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4266
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7431
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 4629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30986
bin: 9.75e1
variant carriers: 2

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-1

FS
type: SiteQuality
SIO_000300: 2.579e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.774472e6

ClippingRankSum
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SIO_000300: -8.4e-1

BaseQRankSum
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SIO_000300: -2.55e0

MQ
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SIO_000300: 5.964e1

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.3e0

QD
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SIO_000300: 1.144e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 2.68e0

QD
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VQSLOD
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DP
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SIO_000300: 2.774468e6

ReadPosRankSum
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SIO_000300: 5.86e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

African
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allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
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SIO_000300: -5.11e-1

DP
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SIO_000300: 2.774685e6

MQRankSum
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SIO_000300: 4.29e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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SIO_000300: 1.283e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.726e1

ReadPosRankSum
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SIO_000300: 9.09e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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BaseQRankSum
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SIO_000300: -6.870000000000001e-1

VQSLOD
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MQRankSum
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SIO_000300: 2.7e-1

DP
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SIO_000300: 2.774489e6

QD
type: SiteQuality
SIO_000300: 1.573e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 9.409999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.993766482857828e-5
allele num: 66736
num of homozygotes: 0

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

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

South Asian
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allele frequency: 8.478682170542636e-4
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993586862057598e-5
allele num: 66738
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

Latino
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allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

East Asian
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South Asian
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allele num: 16512
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African
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allele frequency: 0.0e0
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

South Asian
type: Population
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num of homozygotes: 0

Other
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VQSLOD
type: SiteQuality
SIO_000300: -1.172e-1

DP
type: SiteQuality
SIO_000300: 2.774605e6

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.88e0

BaseQRankSum
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SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.131e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
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MQRankSum
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FS
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ClippingRankSum
type: SiteQuality
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DP
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QD
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SIO_000300: 1.326e1

BaseQRankSum
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SIO_000300: 5.94e0

VQSLOD
type: SiteQuality
SIO_000300: -2.288e0

ReadPosRankSum
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SIO_000300: 1.26e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.169e1

FS
type: SiteQuality
SIO_000300: 3.946e0

DP
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 5.917e1

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 4.668e0

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

VQSLOD
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SIO_000300: 7.17e-1

ReadPosRankSum
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SIO_000300: 1.39e-1

DP
type: SiteQuality
SIO_000300: 2.775664e6

MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.692e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
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FS
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MQ
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

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

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

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

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

African
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

African
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Other
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Latino
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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num of homozygotes: 0

East Asian
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allele frequency: 2.314279102059708e-4
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African
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South Asian
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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QD
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

European (Non-Finnish)
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Other
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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MQ
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FS
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DP
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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Other
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African
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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FS
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QD
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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East Asian
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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East Asian
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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ClippingRankSum
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FS
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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FS
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InbreedingCoeff
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DP
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MQ
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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DP
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: -2.29e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.857e0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493780162465154e-5
allele num: 66722
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 11576
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 1.245e1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 4.916e0

DP
type: SiteQuality
SIO_000300: 1.841849e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.907e0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40557
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 4458
bin: 9.75e1
variant carriers: 3

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

ReadPosRankSum
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SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.841784e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeDepth
all individuals: 9890
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variant carriers: 0

GenotypeDepth
all individuals: 282
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1026
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
all individuals: 688
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variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 4.633e0

DP
type: SiteQuality
SIO_000300: 1.841649e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1937
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GenotypeQuality
all individuals: 4455
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variant carriers: 1

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.902e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

MQ
type: SiteQuality
SIO_000300: 5.869e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 1.454e1

DP
type: SiteQuality
SIO_000300: 1.841278e6

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1024
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.695e0

BaseQRankSum
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.496402877697842e-5
allele num: 66720
num of homozygotes: 0

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

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

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

Other
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South Asian
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BaseQRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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MQ
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SIO_000300: 5.962e1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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Latino
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 3.778e0

MQRankSum
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SIO_000300: 1.12e0

MQ
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SIO_000300: 5.879e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.03e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.839951e6

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 796
allele frequency: 7.650903498654364e-2
allele num: 10404
num of homozygotes: 44

Latino
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allele count: 35
allele frequency: 3.023496890117485e-3
allele num: 11576
num of homozygotes: 1

Other
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allele num: 906
num of homozygotes: 0

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.495352881213648e-5
allele num: 66708
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

DP
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InbreedingCoeff
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MQ
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SIO_000300: 5.97e1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.18e-1

MQRankSum
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SIO_000300: 2.06e-1

ClippingRankSum
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SIO_000300: -2.57e-1

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 16
allele frequency: 2.398512921988367e-4
allele num: 66708
num of homozygotes: 0

Latino
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allele frequency: 3.628196268140981e-3
allele num: 11576
num of homozygotes: 0

African
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allele frequency: 6.354547202461065e-2
allele num: 10402
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.368e1

InbreedingCoeff
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SIO_000300: 4.99e-2

MQRankSum
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DP
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -4.7e-2

BaseQRankSum
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SIO_000300: -1.7e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 6.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Other
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Other
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South Asian
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num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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SIO_000300: 1.817957e6

GenotypeDepth
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variant carriers: 1

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.763e1

BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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Latino
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allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.799856011519078e-4
allele num: 66672
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.5e-3

DP
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MQ
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QD
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SIO_000300: 1.163e1

VQSLOD
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MQRankSum
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SIO_000300: 1.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele num: 11570
num of homozygotes: 0

Other
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FS
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MQ
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

Latino
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BaseQRankSum
type: SiteQuality
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

African
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allele num: 10398
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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DP
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 9.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.421e1

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.504577792453396e-5
allele num: 66626
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8642
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

European (Non-Finnish)
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African
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East Asian
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Other
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European (Finnish)
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Latino
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.095767036925848e-3
allele num: 66620
num of homozygotes: 0

Latino
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allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

Other
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European (Finnish)
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South Asian
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African
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allele num: 10396
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9168
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41528
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3732
bin: 9.75e1
variant carriers: 8

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

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.628558204119417e-4
allele num: 8642
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.373e1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

DP
type: SiteQuality
SIO_000300: 1.811263e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.258e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1786
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 9.75e1
variant carriers: 9

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.787037037037037e-4
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

DP
type: SiteQuality
SIO_000300: 1.810926e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.094e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.063e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

FS
type: SiteQuality
SIO_000300: 1.917e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.87e-1

DP
type: SiteQuality
SIO_000300: 1.810318e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.07e1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.56e-1

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

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
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: 2
allele frequency: 3.003453972067878e-5
allele num: 66590
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 2.759e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

QD
type: SiteQuality
SIO_000300: 1.308e1

DP
type: SiteQuality
SIO_000300: 1.809844e6

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

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

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