19-56312923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312923
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312923
    reference: chr 19
allele count: 5
allele frequency: 4.176760504552669e-5
allele num: 119710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1874+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2171+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2009+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2009+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1874+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2171+15G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2171+15G>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

19-56312924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312924
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312924
    reference: chr 19
allele count: 21
allele frequency: 1.751693303526743e-4
allele num: 119884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2009+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2171+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1874+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2009+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1874+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2171+14C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2171+14C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5927
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/19-56312930-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312930
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312930
    reference: chr 19
allele count: 1
allele frequency: 8.312275568559649e-6
allele num: 120304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2171+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1874+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2009+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2171+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1874+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2171+8G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2009+8G>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35623
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5908
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2171+8G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-56312936-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312936
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312936
    reference: chr 19
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2171+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1874+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2009+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2171+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2171+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2009+2T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1874+2T>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2171+2T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

19-56312943-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312943
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312943
    reference: chr 19
allele count: 2
allele frequency: 1.653575857792476e-5
allele num: 120950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2004T>C
  hgvsp: ENST00000360133.3:c.2004T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2166T>C
  hgvsp: ENST00000443188.1:c.2166T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2004T>C
  hgvsp: ENST00000589824.2:c.2004T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2166T>C
  hgvsp: ENST00000593244.1:c.2166T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1869T>C
  hgvsp: ENST00000592953.1:c.1869T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1869T>C
  hgvsp: ENST00000590409.1:c.1869T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2166T>C
  hgvsp: ENST00000589093.1:c.2166T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His722His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP

19-56312945-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312945
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312945
    reference: chr 19
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2164C>G
  hgvsp: ENSP00000409898.1:p.His722Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1867C>G
  hgvsp: ENSP00000466582.1:p.His623Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2164C>G
  hgvsp: ENSP00000466285.1:p.His722Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1867C>G
  hgvsp: ENSP00000468196.1:p.His623Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2164C>G
  hgvsp: ENSP00000467988.1:p.His722Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.2002C>G
  hgvsp: ENSP00000353251.3:p.His668Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.2002C>G
  hgvsp: ENSP00000468082.1:p.His668Asp
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8478
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His722Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

19-56312951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312951
    reference: chr 19
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1996A>G
  hgvsp: ENSP00000468082.1:p.Ile666Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2158A>G
  hgvsp: ENSP00000409898.1:p.Ile720Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1861A>G
  hgvsp: ENSP00000468196.1:p.Ile621Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1861A>G
  hgvsp: ENSP00000466582.1:p.Ile621Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2158A>G
  hgvsp: ENSP00000467988.1:p.Ile720Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2158A>G
  hgvsp: ENSP00000466285.1:p.Ile720Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1996A>G
  hgvsp: ENSP00000353251.3:p.Ile666Val
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5904
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile720Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

19-56312952-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312952
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312952
    reference: chr 19
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2157A>G
  hgvsp: ENST00000589093.1:c.2157A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2157A>G
  hgvsp: ENST00000443188.1:c.2157A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2157A>G
  hgvsp: ENST00000593244.1:c.2157A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1995A>G
  hgvsp: ENST00000360133.3:c.1995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1860A>G
  hgvsp: ENST00000592953.1:c.1860A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1995A>G
  hgvsp: ENST00000589824.2:c.1995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1860A>G
  hgvsp: ENST00000590409.1:c.1860A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln719Gln
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

19-56312955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312955
    reference: chr 19
allele count: 5
allele frequency: 4.126774513040608e-5
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2154C>T
  hgvsp: ENST00000443188.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1992C>T
  hgvsp: ENST00000589824.2:c.1992C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1992C>T
  hgvsp: ENST00000360133.3:c.1992C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2154C>T
  hgvsp: ENST00000593244.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2154C>T
  hgvsp: ENST00000589093.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1857C>T
  hgvsp: ENST00000592953.1:c.1857C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1857C>T
  hgvsp: ENST00000590409.1:c.1857C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys718Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-56312960-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312960
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312960
    reference: chr 19
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1852A>C
  hgvsp: ENSP00000468196.1:p.Thr618Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1987A>C
  hgvsp: ENSP00000468082.1:p.Thr663Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2149A>C
  hgvsp: ENSP00000467988.1:p.Thr717Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1987A>C
  hgvsp: ENSP00000353251.3:p.Thr663Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2149A>C
  hgvsp: ENSP00000466285.1:p.Thr717Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1852A>C
  hgvsp: ENSP00000466582.1:p.Thr618Pro
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2149A>C
  hgvsp: ENSP00000409898.1:p.Thr717Pro
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr717Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-56312963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312963
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312963
    reference: chr 19
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2146C>T
  hgvsp: ENSP00000467988.1:p.Pro716Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1849C>T
  hgvsp: ENSP00000468196.1:p.Pro617Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1984C>T
  hgvsp: ENSP00000353251.3:p.Pro662Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2146C>T
  hgvsp: ENSP00000466285.1:p.Pro716Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1984C>T
  hgvsp: ENSP00000468082.1:p.Pro662Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2146C>T
  hgvsp: ENSP00000409898.1:p.Pro716Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1849C>T
  hgvsp: ENSP00000466582.1:p.Pro617Ser
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5900
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro716Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

19-56312966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312966
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312966
    reference: chr 19
allele count: 4
allele frequency: 3.297609233305853e-5
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2143G>A
  hgvsp: ENSP00000467988.1:p.Glu715Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1981G>A
  hgvsp: ENSP00000353251.3:p.Glu661Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1981G>A
  hgvsp: ENSP00000468082.1:p.Glu661Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2143G>A
  hgvsp: ENSP00000409898.1:p.Glu715Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2143G>A
  hgvsp: ENSP00000466285.1:p.Glu715Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1846G>A
  hgvsp: ENSP00000466582.1:p.Glu616Lys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1846G>A
  hgvsp: ENSP00000468196.1:p.Glu616Lys
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13683
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5899
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu715Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

19-56312970-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312970
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312970
    reference: chr 19
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1842G>A
  hgvsp: ENST00000592953.1:c.1842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1842G>A
  hgvsp: ENST00000590409.1:c.1842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2139G>A
  hgvsp: ENST00000593244.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2139G>A
  hgvsp: ENST00000589093.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2139G>A
  hgvsp: ENST00000443188.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1977G>A
  hgvsp: ENST00000360133.3:c.1977G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1977G>A
  hgvsp: ENST00000589824.2:c.1977G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu713Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

19-56312973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312973
    reference: chr 19
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1974C>T
  hgvsp: ENST00000589824.2:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2136C>T
  hgvsp: ENST00000589093.1:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2136C>T
  hgvsp: ENST00000593244.1:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1839C>T
  hgvsp: ENST00000590409.1:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1839C>T
  hgvsp: ENST00000592953.1:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1974C>T
  hgvsp: ENST00000360133.3:c.1974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2136C>T
  hgvsp: ENST00000443188.1:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile712Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

19-56312973-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312973
    reference: chr 19
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1974C>G
  hgvsp: ENSP00000353251.3:p.Ile658Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2136C>G
  hgvsp: ENSP00000409898.1:p.Ile712Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2136C>G
  hgvsp: ENSP00000466285.1:p.Ile712Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1974C>G
  hgvsp: ENSP00000468082.1:p.Ile658Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1839C>G
  hgvsp: ENSP00000468196.1:p.Ile613Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1839C>G
  hgvsp: ENSP00000466582.1:p.Ile613Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2136C>G
  hgvsp: ENSP00000467988.1:p.Ile712Met
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile712Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

19-56312973-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312972
    reference: chr 19
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2135delT
  hgvsp: ENSP00000467988.1:p.Ile712ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1973delT
  hgvsp: ENSP00000468082.1:p.Ile658ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1838delT
  hgvsp: ENSP00000468196.1:p.Ile613ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1838delT
  hgvsp: ENSP00000466582.1:p.Ile613ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1973delT
  hgvsp: ENSP00000353251.3:p.Ile658ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2135delT
  hgvsp: ENSP00000466285.1:p.Ile712ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2135delT
  hgvsp: ENSP00000409898.1:p.Ile712ThrfsTer9
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile712ThrfsTer9
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: GA
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

19-56312977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312977
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312977
    reference: chr 19
allele count: 10
allele frequency: 8.239539904091755e-5
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1835A>G
  hgvsp: ENSP00000468196.1:p.Asp612Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2132A>G
  hgvsp: ENSP00000466285.1:p.Asp711Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1835A>G
  hgvsp: ENSP00000466582.1:p.Asp612Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2132A>G
  hgvsp: ENSP00000409898.1:p.Asp711Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1970A>G
  hgvsp: ENSP00000468082.1:p.Asp657Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1970A>G
  hgvsp: ENSP00000353251.3:p.Asp657Gly
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2132A>G
  hgvsp: ENSP00000467988.1:p.Asp711Gly
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp711Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-56312981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312981
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312981
    reference: chr 19
allele count: 16
allele frequency: 1.318174328554951e-4
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2128C>T
  hgvsp: ENSP00000466285.1:p.His710Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2128C>T
  hgvsp: ENSP00000467988.1:p.His710Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2128C>T
  hgvsp: ENSP00000409898.1:p.His710Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1966C>T
  hgvsp: ENSP00000468082.1:p.His656Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1831C>T
  hgvsp: ENSP00000466582.1:p.His611Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1966C>T
  hgvsp: ENSP00000353251.3:p.His656Tyr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1831C>T
  hgvsp: ENSP00000468196.1:p.His611Tyr
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36980
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8512
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His710Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS

19-56312984-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312984
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312984
    reference: chr 19
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1963C>A
  hgvsp: ENSP00000353251.3:p.Leu655Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1828C>A
  hgvsp: ENSP00000466582.1:p.Leu610Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1963C>A
  hgvsp: ENSP00000468082.1:p.Leu655Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2125C>A
  hgvsp: ENSP00000467988.1:p.Leu709Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1828C>A
  hgvsp: ENSP00000468196.1:p.Leu610Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2125C>A
  hgvsp: ENSP00000466285.1:p.Leu709Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2125C>A
  hgvsp: ENSP00000409898.1:p.Leu709Met
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5870
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu709Met
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum

19-56312985-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312985
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312985
    reference: chr 19
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1962T>A
  hgvsp: ENST00000589824.2:c.1962T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2124T>A
  hgvsp: ENST00000443188.1:c.2124T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1827T>A
  hgvsp: ENST00000592953.1:c.1827T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1827T>A
  hgvsp: ENST00000590409.1:c.1827T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2124T>A
  hgvsp: ENST00000589093.1:c.2124T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2124T>A
  hgvsp: ENST00000593244.1:c.2124T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1962T>A
  hgvsp: ENST00000360133.3:c.1962T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8517
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu708Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-56320196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56320196
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56320196
    reference: chr 19
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1483C>T
  hgvsp: ENSP00000468196.1:p.Leu495Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.1780C>T
  hgvsp: ENSP00000467988.1:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1483C>T
  hgvsp: ENSP00000466582.1:p.Leu495Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.1780C>T
  hgvsp: ENSP00000409898.1:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1780C>T
  hgvsp: ENSP00000353251.3:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1780C>T
  hgvsp: ENSP00000468082.1:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.1780C>T
  hgvsp: ENSP00000466285.1:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1719
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39587
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu594Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-56312988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312988
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312988
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1824A>G
  hgvsp: ENST00000592953.1:c.1824A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1824A>G
  hgvsp: ENST00000590409.1:c.1824A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1959A>G
  hgvsp: ENST00000589824.2:c.1959A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2121A>G
  hgvsp: ENST00000593244.1:c.2121A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1959A>G
  hgvsp: ENST00000360133.3:c.1959A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2121A>G
  hgvsp: ENST00000589093.1:c.2121A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2121A>G
  hgvsp: ENST00000443188.1:c.2121A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5868
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser707Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-56312991-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312991
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312991
    reference: chr 19
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1956T>C
  hgvsp: ENST00000360133.3:c.1956T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1956T>C
  hgvsp: ENST00000589824.2:c.1956T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2118T>C
  hgvsp: ENST00000443188.1:c.2118T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1821T>C
  hgvsp: ENST00000590409.1:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2118T>C
  hgvsp: ENST00000589093.1:c.2118T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2118T>C
  hgvsp: ENST00000593244.1:c.2118T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1821T>C
  hgvsp: ENST00000592953.1:c.1821T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe706Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum

19-56312991-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312991
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312991
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2118T>A
  hgvsp: ENSP00000467988.1:p.Phe706Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1956T>A
  hgvsp: ENSP00000353251.3:p.Phe652Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1821T>A
  hgvsp: ENSP00000468196.1:p.Phe607Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1956T>A
  hgvsp: ENSP00000468082.1:p.Phe652Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2118T>A
  hgvsp: ENSP00000466285.1:p.Phe706Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1821T>A
  hgvsp: ENSP00000466582.1:p.Phe607Leu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2118T>A
  hgvsp: ENSP00000409898.1:p.Phe706Leu
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5868
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe706Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-56312994-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312994
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312992
    reference: chr 19
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1816_1817delAT
  hgvsp: ENSP00000468196.1:p.Met606ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1951_1952delAT
  hgvsp: ENSP00000353251.3:p.Met651ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1951_1952delAT
  hgvsp: ENSP00000468082.1:p.Met651ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2113_2114delAT
  hgvsp: ENSP00000467988.1:p.Met705ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1816_1817delAT
  hgvsp: ENSP00000466582.1:p.Met606ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2113_2114delAT
  hgvsp: ENSP00000466285.1:p.Met705ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2113_2114delAT
  hgvsp: ENSP00000409898.1:p.Met705ValfsTer6
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5865
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met705ValfsTer6
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: CAT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS

19-56312997-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56312997
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56312997
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2112T>C
  hgvsp: ENST00000593244.1:c.2112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1950T>C
  hgvsp: ENST00000589824.2:c.1950T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2112T>C
  hgvsp: ENST00000443188.1:c.2112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1815T>C
  hgvsp: ENST00000592953.1:c.1815T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2112T>C
  hgvsp: ENST00000589093.1:c.2112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1815T>C
  hgvsp: ENST00000590409.1:c.1815T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1950T>C
  hgvsp: ENST00000360133.3:c.1950T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5862
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn704Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

19-56313009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313009
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313009
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1803C>T
  hgvsp: ENST00000592953.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1938C>T
  hgvsp: ENST00000589824.2:c.1938C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1803C>T
  hgvsp: ENST00000590409.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2100C>T
  hgvsp: ENST00000593244.1:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2100C>T
  hgvsp: ENST00000443188.1:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1938C>T
  hgvsp: ENST00000360133.3:c.1938C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2100C>T
  hgvsp: ENST00000589093.1:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser700Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/19-56313012-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313012
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2097G>T
  hgvsp: ENST00000589093.1:c.2097G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1935G>T
  hgvsp: ENST00000360133.3:c.1935G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2097G>T
  hgvsp: ENST00000593244.1:c.2097G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2097G>T
  hgvsp: ENST00000443188.1:c.2097G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1800G>T
  hgvsp: ENST00000592953.1:c.1800G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1935G>T
  hgvsp: ENST00000589824.2:c.1935G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1800G>T
  hgvsp: ENST00000590409.1:c.1800G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37016
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8515
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr699Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

19-56313012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313012
    reference: chr 19
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1800G>A
  hgvsp: ENST00000590409.1:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2097G>A
  hgvsp: ENST00000589093.1:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1800G>A
  hgvsp: ENST00000592953.1:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1935G>A
  hgvsp: ENST00000360133.3:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2097G>A
  hgvsp: ENST00000593244.1:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1935G>A
  hgvsp: ENST00000589824.2:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2097G>A
  hgvsp: ENST00000443188.1:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr699Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

19-56313013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313013
    reference: chr 19
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2096C>T
  hgvsp: ENSP00000409898.1:p.Thr699Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2096C>T
  hgvsp: ENSP00000466285.1:p.Thr699Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1934C>T
  hgvsp: ENSP00000353251.3:p.Thr645Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1934C>T
  hgvsp: ENSP00000468082.1:p.Thr645Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2096C>T
  hgvsp: ENSP00000467988.1:p.Thr699Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1799C>T
  hgvsp: ENSP00000468196.1:p.Thr600Met
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1799C>T
  hgvsp: ENSP00000466582.1:p.Thr600Met
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  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: 26488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr699Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

19-56313020-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313020
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313020
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1927A>G
  hgvsp: ENSP00000468082.1:p.Asn643Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1792A>G
  hgvsp: ENSP00000466582.1:p.Asn598Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2089A>G
  hgvsp: ENSP00000467988.1:p.Asn697Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2089A>G
  hgvsp: ENSP00000409898.1:p.Asn697Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1927A>G
  hgvsp: ENSP00000353251.3:p.Asn643Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2089A>G
  hgvsp: ENSP00000466285.1:p.Asn697Asp
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1792A>G
  hgvsp: ENSP00000468196.1:p.Asn598Asp
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  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: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8511
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37027
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn697Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

19-56313029-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313029
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313029
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1918C>G
  hgvsp: ENSP00000353251.3:p.Leu640Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1918C>G
  hgvsp: ENSP00000468082.1:p.Leu640Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2080C>G
  hgvsp: ENSP00000467988.1:p.Leu694Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1783C>G
  hgvsp: ENSP00000468196.1:p.Leu595Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2080C>G
  hgvsp: ENSP00000409898.1:p.Leu694Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1783C>G
  hgvsp: ENSP00000466582.1:p.Leu595Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2080C>G
  hgvsp: ENSP00000466285.1:p.Leu694Val
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37020
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu694Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

19-56313033-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313033
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1914A>G
  hgvsp: ENST00000360133.3:c.1914A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2076A>G
  hgvsp: ENST00000593244.1:c.2076A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2076A>G
  hgvsp: ENST00000443188.1:c.2076A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1914A>G
  hgvsp: ENST00000589824.2:c.1914A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1779A>G
  hgvsp: ENST00000592953.1:c.1779A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2076A>G
  hgvsp: ENST00000589093.1:c.2076A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1779A>G
  hgvsp: ENST00000590409.1:c.1779A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5852
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr692Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

19-56313043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313043
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313043
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1769G>A
  hgvsp: ENSP00000466582.1:p.Arg590Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2066G>A
  hgvsp: ENSP00000467988.1:p.Arg689Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1904G>A
  hgvsp: ENSP00000353251.3:p.Arg635Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2066G>A
  hgvsp: ENSP00000409898.1:p.Arg689Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1904G>A
  hgvsp: ENSP00000468082.1:p.Arg635Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1769G>A
  hgvsp: ENSP00000468196.1:p.Arg590Gln
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2066G>A
  hgvsp: ENSP00000466285.1:p.Arg689Gln
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37004
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5852
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg689Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum

19-56313045-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313045
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313045
    reference: chr 19
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1902T>C
  hgvsp: ENST00000589824.2:c.1902T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1902T>C
  hgvsp: ENST00000360133.3:c.1902T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1767T>C
  hgvsp: ENST00000592953.1:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2064T>C
  hgvsp: ENST00000443188.1:c.2064T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2064T>C
  hgvsp: ENST00000593244.1:c.2064T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2064T>C
  hgvsp: ENST00000589093.1:c.2064T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1767T>C
  hgvsp: ENST00000590409.1:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5851
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn688Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-56313049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313049
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313049
    reference: chr 19
allele count: 9
allele frequency: 7.413631196560076e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1898G>A
  hgvsp: ENSP00000468082.1:p.Arg633His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2060G>A
  hgvsp: ENSP00000467988.1:p.Arg687His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2060G>A
  hgvsp: ENSP00000409898.1:p.Arg687His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2060G>A
  hgvsp: ENSP00000466285.1:p.Arg687His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1763G>A
  hgvsp: ENSP00000466582.1:p.Arg588His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1898G>A
  hgvsp: ENSP00000353251.3:p.Arg633His
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1763G>A
  hgvsp: ENSP00000468196.1:p.Arg588His
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36999
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg687His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-56313063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313063
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313063
    reference: chr 19
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1749C>T
  hgvsp: ENST00000590409.1:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2046C>T
  hgvsp: ENST00000589093.1:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1884C>T
  hgvsp: ENST00000589824.2:c.1884C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2046C>T
  hgvsp: ENST00000443188.1:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1884C>T
  hgvsp: ENST00000360133.3:c.1884C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2046C>T
  hgvsp: ENST00000593244.1:c.2046C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1749C>T
  hgvsp: ENST00000592953.1:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37008
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu682Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-56313067-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313067
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313067
    reference: chr 19
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1745T>C
  hgvsp: ENSP00000466582.1:p.Leu582Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2042T>C
  hgvsp: ENSP00000466285.1:p.Leu681Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1880T>C
  hgvsp: ENSP00000468082.1:p.Leu627Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1745T>C
  hgvsp: ENSP00000468196.1:p.Leu582Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2042T>C
  hgvsp: ENSP00000467988.1:p.Leu681Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1880T>C
  hgvsp: ENSP00000353251.3:p.Leu627Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2042T>C
  hgvsp: ENSP00000409898.1:p.Leu681Ser
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26484
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8504
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu681Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-56313069-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313069
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313069
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2040C>A
  hgvsp: ENSP00000467988.1:p.Asp680Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1878C>A
  hgvsp: ENSP00000468082.1:p.Asp626Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1878C>A
  hgvsp: ENSP00000353251.3:p.Asp626Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2040C>A
  hgvsp: ENSP00000466285.1:p.Asp680Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1743C>A
  hgvsp: ENSP00000468196.1:p.Asp581Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1743C>A
  hgvsp: ENSP00000466582.1:p.Asp581Glu
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2040C>A
  hgvsp: ENSP00000409898.1:p.Asp680Glu
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9714
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp680Glu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

19-56313085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313085
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313085
    reference: chr 19
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2024C>T
  hgvsp: ENSP00000409898.1:p.Ala675Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2024C>T
  hgvsp: ENSP00000466285.1:p.Ala675Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1727C>T
  hgvsp: ENSP00000468196.1:p.Ala576Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1862C>T
  hgvsp: ENSP00000468082.1:p.Ala621Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1862C>T
  hgvsp: ENSP00000353251.3:p.Ala621Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1727C>T
  hgvsp: ENSP00000466582.1:p.Ala576Val
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2024C>T
  hgvsp: ENSP00000467988.1:p.Ala675Val
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36905
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala675Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/19-56313086-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313086
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313086
    reference: chr 19
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1861G>T
  hgvsp: ENSP00000468082.1:p.Ala621Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1726G>T
  hgvsp: ENSP00000468196.1:p.Ala576Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2023G>T
  hgvsp: ENSP00000409898.1:p.Ala675Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2023G>T
  hgvsp: ENSP00000466285.1:p.Ala675Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2023G>T
  hgvsp: ENSP00000467988.1:p.Ala675Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1861G>T
  hgvsp: ENSP00000353251.3:p.Ala621Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1726G>T
  hgvsp: ENSP00000466582.1:p.Ala576Ser
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala675Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

19-56313086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313086
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313086
    reference: chr 19
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1726G>A
  hgvsp: ENSP00000466582.1:p.Ala576Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2023G>A
  hgvsp: ENSP00000467988.1:p.Ala675Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1861G>A
  hgvsp: ENSP00000353251.3:p.Ala621Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2023G>A
  hgvsp: ENSP00000409898.1:p.Ala675Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2023G>A
  hgvsp: ENSP00000466285.1:p.Ala675Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1726G>A
  hgvsp: ENSP00000468196.1:p.Ala576Thr
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1861G>A
  hgvsp: ENSP00000468082.1:p.Ala621Thr
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala675Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

19-56313089-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313089
    reference: chr 19
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2020A>T
  hgvsp: ENSP00000466285.1:p.Thr674Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2020A>T
  hgvsp: ENSP00000409898.1:p.Thr674Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1723A>T
  hgvsp: ENSP00000468196.1:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1858A>T
  hgvsp: ENSP00000468082.1:p.Thr620Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1858A>T
  hgvsp: ENSP00000353251.3:p.Thr620Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1723A>T
  hgvsp: ENSP00000466582.1:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2020A>T
  hgvsp: ENSP00000467988.1:p.Thr674Ser
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr674Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-56313094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313094
    reference: chr 19
allele count: 2
allele frequency: 1.650410126916539e-5
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1718T>C
  hgvsp: ENSP00000468196.1:p.Val573Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1853T>C
  hgvsp: ENSP00000468082.1:p.Val618Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1853T>C
  hgvsp: ENSP00000353251.3:p.Val618Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2015T>C
  hgvsp: ENSP00000467988.1:p.Val672Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2015T>C
  hgvsp: ENSP00000409898.1:p.Val672Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2015T>C
  hgvsp: ENSP00000466285.1:p.Val672Ala
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1718T>C
  hgvsp: ENSP00000466582.1:p.Val573Ala
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5822
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36739
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val672Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

19-56313095-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313095
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313093
    reference: chr 19
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1715_1716delAT
  hgvsp: ENSP00000466582.1:p.Tyr572CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2012_2013delAT
  hgvsp: ENSP00000466285.1:p.Tyr671CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1850_1851delAT
  hgvsp: ENSP00000468082.1:p.Tyr617CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1715_1716delAT
  hgvsp: ENSP00000468196.1:p.Tyr572CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2012_2013delAT
  hgvsp: ENSP00000467988.1:p.Tyr671CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1850_1851delAT
  hgvsp: ENSP00000353251.3:p.Tyr617CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2012_2013delAT
  hgvsp: ENSP00000409898.1:p.Tyr671CysfsTer8
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr671CysfsTer8
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: CAT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

19-56313097-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313097
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313097
    reference: chr 19
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2012A>G
  hgvsp: ENSP00000467988.1:p.Tyr671Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1850A>G
  hgvsp: ENSP00000353251.3:p.Tyr617Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1715A>G
  hgvsp: ENSP00000468196.1:p.Tyr572Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1850A>G
  hgvsp: ENSP00000468082.1:p.Tyr617Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2012A>G
  hgvsp: ENSP00000466285.1:p.Tyr671Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2012A>G
  hgvsp: ENSP00000409898.1:p.Tyr671Cys
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1715A>G
  hgvsp: ENSP00000466582.1:p.Tyr572Cys
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5818
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8386
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr671Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-56313114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313114
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313114
    reference: chr 19
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-9C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-9C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

19-56313121-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313121
    reference: chr 19
allele count: 144
allele frequency: 1.197007481296758e-3
allele num: 120300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-16A>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-16A>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24969
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-56313121-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313121
    reference: chr 19
allele count: 41
allele frequency: 3.408146300914381e-4
allele num: 120300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-16A>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24969
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34605
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

19-56313127-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313127
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313127
    reference: chr 19
allele count: 1
allele frequency: 8.341675008341675e-6
allele num: 119880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-22C>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-22C>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23535
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32209
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

19-56313133-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313133
    reference: chr 19
allele count: 822
allele frequency: 6.873484405050589e-3
allele num: 119590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-28T>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-28T>C
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21814
  bin: 2.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 4.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 2.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 142
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6255
  bin: 9.75e1
  variant carriers: 812
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6907
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 6
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-56313137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313137
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313137
    reference: chr 19
allele count: 1
allele frequency: 8.376472164982996e-6
allele num: 119382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-32C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-32C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19387
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

19-56313138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313138
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313138
    reference: chr 19
allele count: 3
allele frequency: 2.515723270440252e-5
allele num: 119250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-33A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-33A>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4030
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

19-56313142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313142
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313142
    reference: chr 19
allele count: 3
allele frequency: 2.520669489816495e-5
allele num: 119016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-37C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-37C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4036
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22283
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

19-56313150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313150
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313150
    reference: chr 19
allele count: 5
allele frequency: 4.244482173174873e-5
allele num: 117800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-45G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-45G>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4260
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-56313151-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313151
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313148
    reference: chr 19
allele count: 1
allele frequency: 8.475869200386499e-6
allele num: 117982
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-49_2004-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-49_1842-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-49_2004-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-49_1707-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-49_1842-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-49_2004-47delAGA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-49_1707-47delAGA
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: ATCT
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-56313153-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313153
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313154
    reference: chr 19
allele count: 1
allele frequency: 8.510348583877996e-6
allele num: 117504
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-49dupA
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-49dupA
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10595
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-56313156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56313156
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56313156
    reference: chr 19
allele count: 1
allele frequency: 8.543941491088669e-6
allele num: 117042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1842-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1842-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2004-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1707-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1707-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2004-51G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2004-51G>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4078
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5521
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6581
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-56319171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319171
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319171
    reference: chr 19
allele count: 2
allele frequency: 1.702127659574468e-5
allele num: 117500
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+48G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+964G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+48G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+964G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+48G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+48G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+48G>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22041
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

19-56319172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319172
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319172
    reference: chr 19
allele count: 1
allele frequency: 8.501088139281828e-6
allele num: 117632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+47C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+47C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+47C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+963C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+47C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+963C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+47C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8741
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-56319174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319174
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319174
    reference: chr 19
allele count: 2
allele frequency: 1.699350847976073e-5
allele num: 117692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+961A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+45A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+45A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+45A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+45A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+961A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+45A>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8744
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

19-56319177-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319177
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319176
    reference: chr 19
allele count: 1
allele frequency: 8.494300324482272e-6
allele num: 117726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+957delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+957delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+41delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+41delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+41delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+41delG
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+41delG
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22733
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TC
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

19-56319178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319178
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319178
    reference: chr 19
allele count: 3
allele frequency: 2.550022950206552e-5
allele num: 117646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+41G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+41G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+41G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+957G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+41G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+957G>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+41G>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8860
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8744
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-56319181-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319181
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319181
    reference: chr 19
allele count: 1
allele frequency: 8.486947075398038e-6
allele num: 117828
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+38T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+38T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+954T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+38T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+38T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+38T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+954T>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8859
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

19-56319185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319185
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319185
    reference: chr 19
allele count: 1
allele frequency: 8.470269354565475e-6
allele num: 118060
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+34C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+34C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+34C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+950C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+34C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+34C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+950C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4495
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-56319185-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319185
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319185
    reference: chr 19
allele count: 2
allele frequency: 1.694053870913095e-5
allele num: 118060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+34C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+34C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+34C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+34C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+34C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+950C>A
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+950C>A
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4495
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8787
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-56319188-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319188
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319188
    reference: chr 19
allele count: 4
allele frequency: 3.387648633083776e-5
allele num: 118076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+947G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+31G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+31G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+947G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+31G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+31G>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+31G>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23656
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-56319193-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319193
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319193
    reference: chr 19
allele count: 1
allele frequency: 8.443521286117163e-6
allele num: 118434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+942T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+26T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+26T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+942T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+26T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+26T>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+26T>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-56319201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319201
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319201
    reference: chr 19
allele count: 1
allele frequency: 8.39898540256337e-6
allele num: 119062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+18C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+18C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+934C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+18C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+18C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+18C>T
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+934C>T
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8855
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

19-56319203-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319203
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319203
    reference: chr 19
allele count: 1
allele frequency: 8.392500461587526e-6
allele num: 119154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+932A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+932A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+16A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+16A>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

19-56319203-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319203
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319203
    reference: chr 19
allele count: 3
allele frequency: 2.517750138476258e-5
allele num: 119154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+932A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+16A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+16A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+16A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+932A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+16A>C
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+16A>C
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8854
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

19-56319209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56319209
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 56319209
    reference: chr 19
allele count: 9
allele frequency: 7.525712852245172e-5
allele num: 119590
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468082
  ensembl transcript: ENST00000589824
  gene symbol: NLRP11
  hgvsc: ENST00000589824.2:c.1841+926A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466582
  ensembl transcript: ENST00000590409
  gene symbol: NLRP11
  hgvsc: ENST00000590409.1:c.1706+10A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000466285
  ensembl transcript: ENST00000589093
  gene symbol: NLRP11
  hgvsc: ENST00000589093.1:c.2003+10A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000409898
  ensembl transcript: ENST00000443188
  gene symbol: NLRP11
  hgvsc: ENST00000443188.1:c.2003+10A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000467988
  ensembl transcript: ENST00000593244
  gene symbol: NLRP11
  hgvsc: ENST00000593244.1:c.2003+10A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000468196
  ensembl transcript: ENST00000592953
  gene symbol: NLRP11
  hgvsc: ENST00000592953.1:c.1706+10A>G
  variant of: http://identifiers.org/hgnc/22945
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179873
  ensembl protein: ENSP00000353251
  ensembl transcript: ENST00000360133
  gene symbol: NLRP11
  hgvsc: ENST00000360133.3:c.1841+926A>G
  variant of: http://identifiers.org/hgnc/22945
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15003
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34880
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5931
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8323
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.039194371470846e-5
allele num: 66234
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: 10392
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.513809275664408e-5
allele num: 15352
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: 11566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.935614e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

QD
type: SiteQuality
SIO_000300: 1.191e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

GenotypeQuality
all individuals: 1101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2293
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.018139015483053e-4
allele num: 66266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15492
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 6.58e-1

DP
type: SiteQuality
SIO_000300: 1.939102e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.217e1

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 10398
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 2.589e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

DP
type: SiteQuality
SIO_000300: 1.945338e6

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
all individuals: 422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5908
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3078
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66492
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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.246096189881324e-5
allele num: 16010
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.950366e6

QD
type: SiteQuality
SIO_000300: 1.331e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.464e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: -4.732e-1

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36437
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5908
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 862
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004356316659156e-5
allele num: 66570
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: 904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.144e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 2.024e0

DP
type: SiteQuality
SIO_000300: 1.955549e6

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5905
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
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: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.07e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.04e-1

DP
type: SiteQuality
SIO_000300: 1.956261e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.49e-1

FS
type: SiteQuality
SIO_000300: 5.592e0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8485
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36658
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e0

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.958073e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: -2.849e-1

FS
type: SiteQuality
SIO_000300: 8.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 861
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5904
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
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

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

FS
type: SiteQuality
SIO_000300: 7.526e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.346e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.034e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 1.958291e6

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

GenotypeQuality
all individuals: 5903
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Latino
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African
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European (Non-Finnish)
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allele num: 66618
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Other
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MQRankSum
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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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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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Other
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InbreedingCoeff
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FS
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DP
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VQSLOD
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MQRankSum
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QD
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MQ
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ClippingRankSum
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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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Latino
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African
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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African
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Other
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South Asian
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European (Finnish)
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East Asian
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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BaseQRankSum
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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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African
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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East Asian
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MQ
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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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ReadPosRankSum
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FS
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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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African
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East Asian
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66698
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Latino
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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African
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Latino
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South Asian
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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DP
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QD
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ClippingRankSum
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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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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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DP
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 16

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.248538450007495e-4
allele num: 66710
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -4.848e0

MQ
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SIO_000300: 5.969e1

VQSLOD
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SIO_000300: 1.8e0

QD
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SIO_000300: 1.173e1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

DP
type: SiteQuality
SIO_000300: 1.962736e6

FS
type: SiteQuality
SIO_000300: 5.26e-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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
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

ClippingRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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MQRankSum
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SIO_000300: -3.64e-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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Other
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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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

MQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

DP
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SIO_000300: 1.961336e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.114e1

FS
type: SiteQuality
SIO_000300: 4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ReadPosRankSum
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SIO_000300: 2.56e0

VQSLOD
type: SiteQuality
SIO_000300: -3.042e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.284125e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-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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variant carriers: 0

African
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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
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

DP
type: SiteQuality
SIO_000300: 1.961265e6

FS
type: SiteQuality
SIO_000300: 3.847e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.092e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994664748373947e-5
allele num: 66726
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.29e-1

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

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

Other
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allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8654
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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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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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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South Asian
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66730
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Other
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African
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MQRankSum
type: SiteQuality
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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num of homozygotes: 0

East Asian
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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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

MQRankSum
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SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.125e0

FS
type: SiteQuality
SIO_000300: 2.011e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ReadPosRankSum
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SIO_000300: 1.19e0

QD
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SIO_000300: 1.129e1

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.961261e6

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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bin: 8.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
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: 11576
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

BaseQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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DP
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SIO_000300: 1.961261e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10406
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

BaseQRankSum
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SIO_000300: 1.72e0

QD
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SIO_000300: 1.145e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

DP
type: SiteQuality
SIO_000300: 1.961261e6

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
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: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.961261e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.579e0

FS
type: SiteQuality
SIO_000300: 2.565e0

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.96093e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

FS
type: SiteQuality
SIO_000300: 7.474e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.023e0

GenotypeQuality
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variant carriers: 1

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

East Asian
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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
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele 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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.198825151351675e-4
allele num: 66732
num of homozygotes: 0

South Asian
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African
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allele frequency: 9.611687812379854e-5
allele num: 10404
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East Asian
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Other
type: Population
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allele num: 908
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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FS
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BaseQRankSum
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MQRankSum
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SIO_000300: -3.4e-2

MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10402
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East Asian
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allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
SIO_000300: 9.430999999999999e0

MQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66718
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African
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allele frequency: 0.0e0
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East Asian
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allele num: 8654
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Other
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South Asian
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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MQ
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SIO_000300: 5.952e1

InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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SIO_000300: -8.76e-1

VQSLOD
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ClippingRankSum
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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
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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 num: 16508
num of homozygotes: 0

Other
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.959257e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11560
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

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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East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

African
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FS
type: SiteQuality
SIO_000300: 1.063e0

ReadPosRankSum
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.956747e6

QD
type: SiteQuality
SIO_000300: 1.878e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
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 frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
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

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

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
type: SiteQuality
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MQRankSum
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QD
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DP
type: SiteQuality
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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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African
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allele num: 10400
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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European (Finnish)
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African
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Other
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South Asian
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Latino
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MQRankSum
type: SiteQuality
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MQ
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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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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South Asian
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African
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Other
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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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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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Latino
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East Asian
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Other
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 2.271e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

MQ
type: SiteQuality
SIO_000300: 6.04e1

QD
type: SiteQuality
SIO_000300: 1.315e1

DP
type: SiteQuality
SIO_000300: 1.952838e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 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

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 9.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 1.951616e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8171
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
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: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.954e0

QD
type: SiteQuality
SIO_000300: 1.122e1

FS
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 1.93091e6

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5893
bin: 9.75e1
variant carriers: 142

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 34605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1814
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.50385423966363e-4
allele num: 11416
num of homozygotes: 0

African
type: Population
allele count: 140
allele frequency: 1.357904946653734e-2
allele num: 10310
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66288
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.453e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.44e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 5.988e1

DP
type: SiteQuality
SIO_000300: 1.910961e6

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5893
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 1814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 41
allele frequency: 2.53180190193899e-3
allele num: 16194
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
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: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66288
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.453e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.910961e6

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5739
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1776
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.798169980644026e-5
allele num: 11366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.929e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.869057e6

VQSLOD
type: SiteQuality
SIO_000300: -2.716e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
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variant carriers: 1

GenotypeQuality
all individuals: 1527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1676
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 695
allele frequency: 1.052838877779798e-2
allele num: 66012
num of homozygotes: 4

South Asian
type: Population
allele count: 1
allele frequency: 6.243756243756244e-5
allele num: 16016
num of homozygotes: 0

Latino
type: Population
allele count: 73
allele frequency: 6.457891012031139e-3
allele num: 11304
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 23
allele frequency: 3.49969567863664e-3
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 30
allele frequency: 2.924546695262234e-3
allele num: 10258
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.826881e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.428e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

GenotypeQuality
all individuals: 4246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2765
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5531
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 825
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516852228255923e-5
allele num: 65926
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.761225e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.938e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.253e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

GenotypeQuality
all individuals: 1842
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6123
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23394
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5530
bin: 9.75e1
variant carriers: 3

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.554148829583751e-5
allele num: 65874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15918
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.209e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.739956e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.95e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

GenotypeQuality
all individuals: 556
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5527
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.560795402718234e-5
allele num: 65778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 1.713192e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

GenotypeQuality
all individuals: 2332
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6380
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5525
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12597
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.415191172696946e-5
allele num: 15588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.758505829169641e-4
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.044e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 1.011e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 1.633815e6

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.662e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530690341343946e-5
allele num: 65330
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11076
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.553e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.632604e6

MQ
type: SiteQuality
SIO_000300: 5.635e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-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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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15526
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535673700052213e-5
allele num: 65118
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 count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.624505e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.748e1

MQ
type: SiteQuality
SIO_000300: 5.995e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e-1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64874
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.476683937823834e-5
allele num: 15440
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10994
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.599e0

MQRankSum
type: SiteQuality
SIO_000300: -1.733e0

VQSLOD
type: SiteQuality
SIO_000300: -6.322e-1

DP
type: SiteQuality
SIO_000300: 1.615727e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524901643843972e-5
allele num: 65578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14022
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.624000000000001e0

DP
type: SiteQuality
SIO_000300: 1.989039e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.037e1

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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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523647001462701e-5
allele num: 65632
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14080
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

DP
type: SiteQuality
SIO_000300: 1.9897e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 1.906e0

MQRankSum
type: SiteQuality
SIO_000300: -1.077e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.256e1

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046829773620548e-5
allele num: 65642
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14122
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.782e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.425e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523136442562525e-5
allele num: 65654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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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variant carriers: 0

Latino
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allele count: 2
allele frequency: 1.73550850399167e-4
allele num: 11524
num of homozygotes: 0

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

East Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.523461304082876e-5
allele num: 65640
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

QD
type: SiteQuality
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522626225714112e-5
allele num: 65676
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 14212
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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VQSLOD
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DP
type: SiteQuality
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QD
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520265134239411e-5
allele num: 65778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14308
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.736e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

DP
type: SiteQuality
SIO_000300: 2.000939e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.507e0

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8860
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23457
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 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: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.040530268478823e-5
allele num: 65778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.507e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

DP
type: SiteQuality
SIO_000300: 2.000939e6

FS
type: SiteQuality
SIO_000300: 1.736e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8858
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3205
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.040345383235536e-5
allele num: 65782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.396843134515994e-4
allele num: 14318
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 1.176e1

DP
type: SiteQuality
SIO_000300: 2.004048e6

FS
type: SiteQuality
SIO_000300: 9.217000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

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

GenotypeQuality
all individuals: 4496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.865302759851709e-5
allele num: 14566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65876
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: 876
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.011e0

DP
type: SiteQuality
SIO_000300: 2.01043e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

QD
type: SiteQuality
SIO_000300: 1.665e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8906
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514050387596899e-5
allele num: 66048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14990
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.021332e6

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.305e0

QD
type: SiteQuality
SIO_000300: 1.283e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

FS
type: SiteQuality
SIO_000300: 1.813e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.74e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8854
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8904
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
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: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15056
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

DP
type: SiteQuality
SIO_000300: 2.023654e6

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.989e1

QD
type: SiteQuality
SIO_000300: 1.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

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

GenotypeQuality
all individuals: 2238
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4498
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

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

GenotypeQuality
all individuals: 3230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.540501271340356e-5
allele num: 66072
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15056
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.989e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.357e1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 2.023654e6